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Most recent job postings at proclinical
via Proclinical
posted_at: 2 days agoschedule_type: Contractor
QC Chemist - Contract - Onsite
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company. This is a contract role located in Zebulon, NC...
Skills & Requirements:
• Preferred qualifications: proficiency with HPLC equipment.
• Experience of providing QC testing support to at least one value stream.
• Developing knowledge and application of the Quality Management System (QMS)
• Understanding of laboratory practices
QC Chemist - Contract - Onsite
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company. This is a contract role located in Zebulon, NC...
Skills & Requirements:
• Preferred qualifications: proficiency with HPLC equipment.
• Experience of providing QC testing support to at least one value stream.
• Developing knowledge and application of the Quality Management System (QMS)
• Understanding of laboratory practices and testing
• Operational knowledge of analytical chemistry/microbiology (as applicable) laboratory equipment, raising up concerns or issues to ensure diagnosis of problems and identify appropriate actions.
• Full understanding of the requirements and application of GMP principles in a laboratory environment.
• Good verbal and written communication on an individual and group basis targeted to appropriately audiences of several levels within GMS.
• Supports other teams when required.
• Maintain appropriate documentation of training activities
The QC Chemist will:
• Conduct routine analytical testing of raw materials, packaging materials, finished products, and environmental samples using approved methods and various instrumentation (e.g., HPLC, Vitek, GC, UV, microscope, gram stainer, robotics).
• Generate valid data at expected levels of productivity while adhering to cGMP.
• Interpret the validity of own test data and generate accurate results.
• Advise the immediate supervisor or designee of all important aspects of analytical testing including deviations.
• Evaluate data generated by others in the analytical group.
• Accurately document analytical data and review official laboratory documents (e.g., SOPs, technical reports, methods, specifications).
• Assist in analytical method development/validation/transfer.
• Maintain and troubleshoot laboratory instruments.
• Assist in training other laboratory personnel on methods, instrumentation, and computer systems.
• Review and revise training materials.
• Maintain appropriate documentation of training activities.
• Participate in interdepartmental project teams or committees.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCQA Show more details...
Proclinical Staffing is seeking a QC Chemist to join an ambitious pharmaceutical company. This is a contract role located in Zebulon, NC...
Skills & Requirements:
• Preferred qualifications: proficiency with HPLC equipment.
• Experience of providing QC testing support to at least one value stream.
• Developing knowledge and application of the Quality Management System (QMS)
• Understanding of laboratory practices and testing
• Operational knowledge of analytical chemistry/microbiology (as applicable) laboratory equipment, raising up concerns or issues to ensure diagnosis of problems and identify appropriate actions.
• Full understanding of the requirements and application of GMP principles in a laboratory environment.
• Good verbal and written communication on an individual and group basis targeted to appropriately audiences of several levels within GMS.
• Supports other teams when required.
• Maintain appropriate documentation of training activities
The QC Chemist will:
• Conduct routine analytical testing of raw materials, packaging materials, finished products, and environmental samples using approved methods and various instrumentation (e.g., HPLC, Vitek, GC, UV, microscope, gram stainer, robotics).
• Generate valid data at expected levels of productivity while adhering to cGMP.
• Interpret the validity of own test data and generate accurate results.
• Advise the immediate supervisor or designee of all important aspects of analytical testing including deviations.
• Evaluate data generated by others in the analytical group.
• Accurately document analytical data and review official laboratory documents (e.g., SOPs, technical reports, methods, specifications).
• Assist in analytical method development/validation/transfer.
• Maintain and troubleshoot laboratory instruments.
• Assist in training other laboratory personnel on methods, instrumentation, and computer systems.
• Review and revise training materials.
• Maintain appropriate documentation of training activities.
• Participate in interdepartmental project teams or committees.
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCQA Show more details...
via Proclinical
posted_at: 2 days agoschedule_type: Full-time
General Counsel (SVP, Head of Legal & IP) - Permanent - Remote
Proclinical Staffing is seeking a General Counsel (SVP, Head of Legal & IP) to join a world-class biopharmaceutical company. This is a permanent role with the opportunity to work remotely...
Primary Responsibilities
The General Counsel assumes a pivotal role in directing corporate strategic and tactical legal initiatives, business development, and daily operations. Serving as a strategic
General Counsel (SVP, Head of Legal & IP) - Permanent - Remote
Proclinical Staffing is seeking a General Counsel (SVP, Head of Legal & IP) to join a world-class biopharmaceutical company. This is a permanent role with the opportunity to work remotely...
Primary Responsibilities
The General Counsel assumes a pivotal role in directing corporate strategic and tactical legal initiatives, business development, and daily operations. Serving as a strategic partner, this position offers senior management effective guidance on company strategies and their execution, overseeing all aspects of the global legal and intellectual property (IP) function.
Skills & Requirements:
• Juris Doctor/LLM or equivalent degree from an ABA (American Bar Association)-accredited law school or equivalent institution; excellent academic credentials.
• Admitted and in good standing with an appropriate bar.
• Global perspective and experience as a group/corporate Legal & IP head.
• 15+ years of legal and/or IP relevant experience, including corporate in-house experience in MNCs of the Pharmaceutical industry or a prominent American law firm.
• Broad legal knowledge in corporate law, litigations, labor law, IP, etc.
• Customer-focused with the ability to provide legal & IP solutions as a business partner.
• Strong multitasking ability in a fast-paced environment.
• Negotiation skills in legal, commercial, and employment matters.
• Extensive experience in people management.
The General Counsel (SVP, Head of Legal & IP) will:
• Legal Strategy and Advice:
• Develops and executes legal strategies aligned with the company's business objectives.
• Provides timely, pragmatic legal advice and guidance on the legal implications of all matters to the Board of Directors and senior management.
• Reviews, analyzes, and interprets statutes, regulations, policies, decisions, and administrative or judicial opinions of or relating to regulatory and quasi-regulatory bodies to determine potential impacts on the Company.
• Provides legal and IP advising/risk analysis for corporate strategy, business development projects, and operations.
• Corporate Governance and Compliance:
• Oversees corporate governance matters, ensuring compliance with laws and regulations.
• Collaborates with stakeholders to implement and maintain effective compliance programs.
• Presents and leads discussions on legal matters at Board meetings.
• Intellectual Property:
• Manages and secures domestic and international patents, trademarks, copyrights, trade secrets, enforcement, and licensing.
• Prepares and prosecutes patent applications, providing IP guidance on filing and prosecution strategy.
• Conducts IP due diligence and supports business development activities.
• Drafts, reviews, and revises intellectual property-related agreements.
• Litigation Management:
• Manages and oversees litigation matters, working closely with outside counsel if necessary.
• Develops and implements strategies to minimize legal exposure and costs.
• Assesses the merits of litigation against the company and approves settlements where warranted.
• Business Development, Mergers and Acquisitions, Business Transactions:
• Collaborates on legal aspects of business development, mergers, acquisitions, and strategic transactions.
• Conducts due diligence, provides legal counsel, and represents the Company during negotiations.
• Reviews, drafts, and negotiates various contracts, including vendor agreements, partnerships, and licensing agreements.
• Risk Management:
• Identifies and assesses legal risks associated with business activities.
• Implements proactive risk mitigation strategies and processes.
• Develops an Enterprise Risk Management process.
• Leadership and Management of Legal & IP Department:
• Develops and executes business plans for the Legal & IP Department.
• Provides operational oversight and develops, retains, and motivates a team of legal professionals.
• Ensures effective service and value from outside counsel.
• Determines department budget and manages resources efficiently.
If you are having difficulty in applying or if you have any questions, please contact Oliver Jones at +49 69 506077054 or o.jones@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer Show more details...
Proclinical Staffing is seeking a General Counsel (SVP, Head of Legal & IP) to join a world-class biopharmaceutical company. This is a permanent role with the opportunity to work remotely...
Primary Responsibilities
The General Counsel assumes a pivotal role in directing corporate strategic and tactical legal initiatives, business development, and daily operations. Serving as a strategic partner, this position offers senior management effective guidance on company strategies and their execution, overseeing all aspects of the global legal and intellectual property (IP) function.
Skills & Requirements:
• Juris Doctor/LLM or equivalent degree from an ABA (American Bar Association)-accredited law school or equivalent institution; excellent academic credentials.
• Admitted and in good standing with an appropriate bar.
• Global perspective and experience as a group/corporate Legal & IP head.
• 15+ years of legal and/or IP relevant experience, including corporate in-house experience in MNCs of the Pharmaceutical industry or a prominent American law firm.
• Broad legal knowledge in corporate law, litigations, labor law, IP, etc.
• Customer-focused with the ability to provide legal & IP solutions as a business partner.
• Strong multitasking ability in a fast-paced environment.
• Negotiation skills in legal, commercial, and employment matters.
• Extensive experience in people management.
The General Counsel (SVP, Head of Legal & IP) will:
• Legal Strategy and Advice:
• Develops and executes legal strategies aligned with the company's business objectives.
• Provides timely, pragmatic legal advice and guidance on the legal implications of all matters to the Board of Directors and senior management.
• Reviews, analyzes, and interprets statutes, regulations, policies, decisions, and administrative or judicial opinions of or relating to regulatory and quasi-regulatory bodies to determine potential impacts on the Company.
• Provides legal and IP advising/risk analysis for corporate strategy, business development projects, and operations.
• Corporate Governance and Compliance:
• Oversees corporate governance matters, ensuring compliance with laws and regulations.
• Collaborates with stakeholders to implement and maintain effective compliance programs.
• Presents and leads discussions on legal matters at Board meetings.
• Intellectual Property:
• Manages and secures domestic and international patents, trademarks, copyrights, trade secrets, enforcement, and licensing.
• Prepares and prosecutes patent applications, providing IP guidance on filing and prosecution strategy.
• Conducts IP due diligence and supports business development activities.
• Drafts, reviews, and revises intellectual property-related agreements.
• Litigation Management:
• Manages and oversees litigation matters, working closely with outside counsel if necessary.
• Develops and implements strategies to minimize legal exposure and costs.
• Assesses the merits of litigation against the company and approves settlements where warranted.
• Business Development, Mergers and Acquisitions, Business Transactions:
• Collaborates on legal aspects of business development, mergers, acquisitions, and strategic transactions.
• Conducts due diligence, provides legal counsel, and represents the Company during negotiations.
• Reviews, drafts, and negotiates various contracts, including vendor agreements, partnerships, and licensing agreements.
• Risk Management:
• Identifies and assesses legal risks associated with business activities.
• Implements proactive risk mitigation strategies and processes.
• Develops an Enterprise Risk Management process.
• Leadership and Management of Legal & IP Department:
• Develops and executes business plans for the Legal & IP Department.
• Provides operational oversight and develops, retains, and motivates a team of legal professionals.
• Ensures effective service and value from outside counsel.
• Determines department budget and manages resources efficiently.
If you are having difficulty in applying or if you have any questions, please contact Oliver Jones at +49 69 506077054 or o.jones@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer Show more details...
via Proclinical
posted_at: 2 days agoschedule_type: Contractor
Laboratory Assistant - Contract - Onsite
Proclinical Staffing is seeking a Laboratory Assistant to join a leading laboratory. This is a contract role located in Rochester, NY...
The Laboratory Assistant will:
• Perform isolation and cryopreservation of peripheral blood mononuclear cells (PBMC) and bone marrow mononuclear cells (BMMC).
• Perform flow cytometry analysis for PBMCs and BMMCs, as required.
• Monitor reagent and supply inventory
Laboratory Assistant - Contract - Onsite
Proclinical Staffing is seeking a Laboratory Assistant to join a leading laboratory. This is a contract role located in Rochester, NY...
The Laboratory Assistant will:
• Perform isolation and cryopreservation of peripheral blood mononuclear cells (PBMC) and bone marrow mononuclear cells (BMMC).
• Perform flow cytometry analysis for PBMCs and BMMCs, as required.
• Monitor reagent and supply inventory for processes related to the essential functions.
• Record all results, lot numbers and associated calculations for all processes related to the essential functions.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at (+1) 857-366-4011 or a.maldonado@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCR Show more details...
Proclinical Staffing is seeking a Laboratory Assistant to join a leading laboratory. This is a contract role located in Rochester, NY...
The Laboratory Assistant will:
• Perform isolation and cryopreservation of peripheral blood mononuclear cells (PBMC) and bone marrow mononuclear cells (BMMC).
• Perform flow cytometry analysis for PBMCs and BMMCs, as required.
• Monitor reagent and supply inventory for processes related to the essential functions.
• Record all results, lot numbers and associated calculations for all processes related to the essential functions.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at (+1) 857-366-4011 or a.maldonado@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCR Show more details...
via Proclinical
posted_at: 2 days agoschedule_type: Full-time
VP of Biology & Immunology - Permanent - Onsite
Proclinical is seeking VP of Biology & Immunology to join a biotech leveraging a high powered computation platform to discover and develop small molecule therapeutics against high value immunological targets. This is a permanent role located in Princeton, NJ...
Skills & Requirements:
• A Ph.D. in biochemistry, cell biology, pharmacology or related field with 10+ years relevant pharmaceutical or biotech
VP of Biology & Immunology - Permanent - Onsite
Proclinical is seeking VP of Biology & Immunology to join a biotech leveraging a high powered computation platform to discover and develop small molecule therapeutics against high value immunological targets. This is a permanent role located in Princeton, NJ...
Skills & Requirements:
• A Ph.D. in biochemistry, cell biology, pharmacology or related field with 10+ years relevant pharmaceutical or biotech experience
• A strong background in immunology drug discovery
• Experience in leading multiple drug discovery programs and/or significant experience as a functional area representative on cross-functional teams
• Demonstrated accomplishments in identifying clinical candidates
• Experience in identifying high-value therapeutic targets in multiple disease areas, based on the evaluation of biological rationale, tractability, and competitive landscape
• Expertise establishing in vitro biochemical/biophysical and cell-based assays and identifying translational disease model
• Experience working with contract research organizations (CRO) on program execution
• Excellent presentation and communication skills
The VP of Biology & Immunology will:
• Leadership of the biology team and function
• Lead drug discovery programs in effective collaboration with multi-disciplinary teams
• Manage CRO scientists to ensure timely delivery of quality scientific data
• Responsible for data review, analysis and interpretation of in vitro and in vivo results, and troubleshooting issues related to drug discovery projects
• Provide strategic input to target selection and portfolio construction
If you are having difficulty in applying or if you have any questions, please contact Max Robinson at (+1) 857-362-9542 or m.robinson@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDSCIC Show more details...
Proclinical is seeking VP of Biology & Immunology to join a biotech leveraging a high powered computation platform to discover and develop small molecule therapeutics against high value immunological targets. This is a permanent role located in Princeton, NJ...
Skills & Requirements:
• A Ph.D. in biochemistry, cell biology, pharmacology or related field with 10+ years relevant pharmaceutical or biotech experience
• A strong background in immunology drug discovery
• Experience in leading multiple drug discovery programs and/or significant experience as a functional area representative on cross-functional teams
• Demonstrated accomplishments in identifying clinical candidates
• Experience in identifying high-value therapeutic targets in multiple disease areas, based on the evaluation of biological rationale, tractability, and competitive landscape
• Expertise establishing in vitro biochemical/biophysical and cell-based assays and identifying translational disease model
• Experience working with contract research organizations (CRO) on program execution
• Excellent presentation and communication skills
The VP of Biology & Immunology will:
• Leadership of the biology team and function
• Lead drug discovery programs in effective collaboration with multi-disciplinary teams
• Manage CRO scientists to ensure timely delivery of quality scientific data
• Responsible for data review, analysis and interpretation of in vitro and in vivo results, and troubleshooting issues related to drug discovery projects
• Provide strategic input to target selection and portfolio construction
If you are having difficulty in applying or if you have any questions, please contact Max Robinson at (+1) 857-362-9542 or m.robinson@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDSCIC Show more details...
via Proclinical
posted_at: 3 days agoschedule_type: Contractor
Executive Assistant - Contract - Onsite
Proclinical Staffing is seeking an Executive Assistant to join a cutting-edge biotech company. This is a contract role located in New Providence, NJ...
The Executive Assistant will:
• General administrative support to other CMO leaders.
• Responsible for proactively coordinating meetings from invite to presentation preparation.
• Arrange and book complex and detailed travel plans for both domestic and
Executive Assistant - Contract - Onsite
Proclinical Staffing is seeking an Executive Assistant to join a cutting-edge biotech company. This is a contract role located in New Providence, NJ...
The Executive Assistant will:
• General administrative support to other CMO leaders.
• Responsible for proactively coordinating meetings from invite to presentation preparation.
• Arrange and book complex and detailed travel plans for both domestic and international travel, creating itineraries and agendas and compiling documents for travel-related meetings and industry conferences.
• Create and submit expense reports via Concur for the CMO and other leaders as needed.
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at (+1) 267-297-3257 or j.jones@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA Show more details...
Proclinical Staffing is seeking an Executive Assistant to join a cutting-edge biotech company. This is a contract role located in New Providence, NJ...
The Executive Assistant will:
• General administrative support to other CMO leaders.
• Responsible for proactively coordinating meetings from invite to presentation preparation.
• Arrange and book complex and detailed travel plans for both domestic and international travel, creating itineraries and agendas and compiling documents for travel-related meetings and industry conferences.
• Create and submit expense reports via Concur for the CMO and other leaders as needed.
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at (+1) 267-297-3257 or j.jones@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA Show more details...
via Proclinical
posted_at: 2 days agoschedule_type: Full-time
Associate Director, Process Chemistry - Permanent - Onsite
Proclinical Staffing is seeking an Associate Director, Process Chemistry to join a cutting-edge CDMO. This is a permanent role located in Philadelphia, PA...
Skills & Requirements:
• This position required PhD degree in Organic Chemistry or Chemical Engineering and at least 8 work experience as process research and development chemist in an industry laboratory.
• Experience with use
Associate Director, Process Chemistry - Permanent - Onsite
Proclinical Staffing is seeking an Associate Director, Process Chemistry to join a cutting-edge CDMO. This is a permanent role located in Philadelphia, PA...
Skills & Requirements:
• This position required PhD degree in Organic Chemistry or Chemical Engineering and at least 8 work experience as process research and development chemist in an industry laboratory.
• Experience with use of jacketed glass reactors up to 100 L
• Experience with common process scale crystallization techniques
• Experience with process scale medium-pressure and high-pressure chromatography development and scale-up
• Experienced with process safety evaluations, i.e. thermal stability analysis
• Knowledge and experience in a GMP environment preferred.
• Knowledge and experience of analytical techniques and compound characterization.
• Excellent oral and written communication/interpersonal skills; ability to speak clearly and persuasively in positive or negative situations with demonstrated leadership with both internal and external customers.
• Strong capability in MS Office suite and working with electronic lab notebook systems (ELN). ERP system use is a plus.
• Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time.
• Frequently lift and or move objects up to 30 pounds.
• Stand/walk during entire length of shift.
• Use arms, hands, and fingers to handle, feel or reach.
• Ability to climb, balance, stoop, kneel, crouch, or crawl.
• Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus.
• Ability to use a PAPR and gown during work with high potent materials.
The Associate Director, Process Chemistry will:
• Leading a team in the development of new processes to manufacture Active Pharmaceutical Ingredient (API) for early development through Phase II clinical trials.
• Ensuring that processes are suitable for controlling the quality of API as required by cGMP, ICH and FDA regulations as well as the attributes conducive to successful formulation development.
• Managing the chemical process development, kilo-lab and pilot plant scale-up of API with contributions to broader CMC and regulatory activities.
• Responsible for contributing to the planning of synthetic routes, the execution and of chemical synthesis projects.
• The preparation, purification, and characterization of all materials, maintaining clear and current records of your work within a laboratory notebook, performing analytical work, attending and contributing to meetings, writing comprehensive reports and purchasing all necessary supplies and equipment.
• Maintain a safe, pleasant, and efficient working environment.
• Thorough documentation and authoring of SOPs, investigations, lab notebooks, batch records, deviations, CAPA and other relevant tech documents as applicable.
• Follow safety procedures for organizational policies
• Identify opportunities for improvement or optimization in current processes and implement viable solutions Investigate route modifications to limit cytotoxicity until the final step to reduce the cost of goods and increasing overall safety.
• Exhibit detailed record-keeping, data analysis and chain of custody controls required in successful implementation of GMP.
• Perform other duties as assigned.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at (+1) 267-428-7770 or m.raletz@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDSCIC Show more details...
Proclinical Staffing is seeking an Associate Director, Process Chemistry to join a cutting-edge CDMO. This is a permanent role located in Philadelphia, PA...
Skills & Requirements:
• This position required PhD degree in Organic Chemistry or Chemical Engineering and at least 8 work experience as process research and development chemist in an industry laboratory.
• Experience with use of jacketed glass reactors up to 100 L
• Experience with common process scale crystallization techniques
• Experience with process scale medium-pressure and high-pressure chromatography development and scale-up
• Experienced with process safety evaluations, i.e. thermal stability analysis
• Knowledge and experience in a GMP environment preferred.
• Knowledge and experience of analytical techniques and compound characterization.
• Excellent oral and written communication/interpersonal skills; ability to speak clearly and persuasively in positive or negative situations with demonstrated leadership with both internal and external customers.
• Strong capability in MS Office suite and working with electronic lab notebook systems (ELN). ERP system use is a plus.
• Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time.
• Frequently lift and or move objects up to 30 pounds.
• Stand/walk during entire length of shift.
• Use arms, hands, and fingers to handle, feel or reach.
• Ability to climb, balance, stoop, kneel, crouch, or crawl.
• Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus.
• Ability to use a PAPR and gown during work with high potent materials.
The Associate Director, Process Chemistry will:
• Leading a team in the development of new processes to manufacture Active Pharmaceutical Ingredient (API) for early development through Phase II clinical trials.
• Ensuring that processes are suitable for controlling the quality of API as required by cGMP, ICH and FDA regulations as well as the attributes conducive to successful formulation development.
• Managing the chemical process development, kilo-lab and pilot plant scale-up of API with contributions to broader CMC and regulatory activities.
• Responsible for contributing to the planning of synthetic routes, the execution and of chemical synthesis projects.
• The preparation, purification, and characterization of all materials, maintaining clear and current records of your work within a laboratory notebook, performing analytical work, attending and contributing to meetings, writing comprehensive reports and purchasing all necessary supplies and equipment.
• Maintain a safe, pleasant, and efficient working environment.
• Thorough documentation and authoring of SOPs, investigations, lab notebooks, batch records, deviations, CAPA and other relevant tech documents as applicable.
• Follow safety procedures for organizational policies
• Identify opportunities for improvement or optimization in current processes and implement viable solutions Investigate route modifications to limit cytotoxicity until the final step to reduce the cost of goods and increasing overall safety.
• Exhibit detailed record-keeping, data analysis and chain of custody controls required in successful implementation of GMP.
• Perform other duties as assigned.
If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at (+1) 267-428-7770 or m.raletz@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDSCIC Show more details...
via Proclinical
posted_at: 3 days agoschedule_type: Contractor
Rebate Analyst - Contract - Onsite
Proclinical Staffing is seeking a Rebate Analyst to join a global pharmaceutical company. This is a contract role located in Plainsboro, NJ...
The Rebate Analyst will:
• Design and develops ad-hoc reports using advanced query techniques for customers; provides analysis and interpretation of the report data
• Designs and develops key metric reports
• Provides reports for federal and state reporting
• Ensure
Rebate Analyst - Contract - Onsite
Proclinical Staffing is seeking a Rebate Analyst to join a global pharmaceutical company. This is a contract role located in Plainsboro, NJ...
The Rebate Analyst will:
• Design and develops ad-hoc reports using advanced query techniques for customers; provides analysis and interpretation of the report data
• Designs and develops key metric reports
• Provides reports for federal and state reporting
• Ensure distribution of daily, weekly and monthly pre-established on-going reports and dashboards in line with business needs and objectives
Compensation:
$30 - $35 per hour
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA Show more details...
Proclinical Staffing is seeking a Rebate Analyst to join a global pharmaceutical company. This is a contract role located in Plainsboro, NJ...
The Rebate Analyst will:
• Design and develops ad-hoc reports using advanced query techniques for customers; provides analysis and interpretation of the report data
• Designs and develops key metric reports
• Provides reports for federal and state reporting
• Ensure distribution of daily, weekly and monthly pre-established on-going reports and dashboards in line with business needs and objectives
Compensation:
$30 - $35 per hour
If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA Show more details...
via Proclinical
posted_at: 3 days agoschedule_type: Contractor
Senior Specialist/Manager, Shipping & Logistics II - Contract - Onsite
Proclinical Staffing is seeking a Senior Specialist/Manager, Shipping & Logistics II to join a cutting-edge pharmaceutical company. This is a contract role located in Lexington, MA...
Primary Responsibilities
The successful candidate will be responsible for the shipping and storage of critical starting materials, drug substance, drug product, and research material. This role
Senior Specialist/Manager, Shipping & Logistics II - Contract - Onsite
Proclinical Staffing is seeking a Senior Specialist/Manager, Shipping & Logistics II to join a cutting-edge pharmaceutical company. This is a contract role located in Lexington, MA...
Primary Responsibilities
The successful candidate will be responsible for the shipping and storage of critical starting materials, drug substance, drug product, and research material. This role requires a strong understanding of GxP environments and familiarity with various CFRs.
Skills & Requirements:
• A Bachelor's degree in Business/Supply Chain or a related subject.
• A minimum of 3 years of experience working in logistics for Pharma/Biotech, with GxP, GDP experience.
• Experience in managing shipping material from external suppliers.
• Experience with temperature-controlled shipments.
• Knowledge of tax and customs duties strategies.
• Detailed knowledge of import/export requirements.
• Strong interpersonal skills and business acumen
The Senior Specialist/Manager, Shipping & Logistics II will:
• Scheduling, executing, and tracking domestic and international shipments of lab samples, raw material, drug substance, and drug product.
• Demonstrating strong knowledge of proper shipping documentation, process, and requirements for international shipments.
• Ensuring accurate valuation of material and proper tariff codes.
• Resolving logistics issues with freight forwarders and customs brokers.
• Analyzing temperature data and managing inventory.
Compensation:
$45 - $60 hourly
If you are having difficulty in applying or if you have any questions, please contact Jay Bastien at (+1) 857-254-1065 or j.bastien@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDOA Show more details...
Proclinical Staffing is seeking a Senior Specialist/Manager, Shipping & Logistics II to join a cutting-edge pharmaceutical company. This is a contract role located in Lexington, MA...
Primary Responsibilities
The successful candidate will be responsible for the shipping and storage of critical starting materials, drug substance, drug product, and research material. This role requires a strong understanding of GxP environments and familiarity with various CFRs.
Skills & Requirements:
• A Bachelor's degree in Business/Supply Chain or a related subject.
• A minimum of 3 years of experience working in logistics for Pharma/Biotech, with GxP, GDP experience.
• Experience in managing shipping material from external suppliers.
• Experience with temperature-controlled shipments.
• Knowledge of tax and customs duties strategies.
• Detailed knowledge of import/export requirements.
• Strong interpersonal skills and business acumen
The Senior Specialist/Manager, Shipping & Logistics II will:
• Scheduling, executing, and tracking domestic and international shipments of lab samples, raw material, drug substance, and drug product.
• Demonstrating strong knowledge of proper shipping documentation, process, and requirements for international shipments.
• Ensuring accurate valuation of material and proper tariff codes.
• Resolving logistics issues with freight forwarders and customs brokers.
• Analyzing temperature data and managing inventory.
Compensation:
$45 - $60 hourly
If you are having difficulty in applying or if you have any questions, please contact Jay Bastien at (+1) 857-254-1065 or j.bastien@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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