Scientist - Quality Control & Analytical Product Development
Bcforward
Scientist - Quality Control & Analytical Product Development
Location: Somerset, NJDuration: 6+ months ContractJob Type: Contract
Key Responsibilities
Analytical Testing: Perform assays, dissolution, hardness tests, water content, content/blend uniformity, and related substances using wet chemistry as per compendial monographs. Laboratory Analysis: Conduct analytical testing of excipients, APIs, in-process, and finished pharmaceutical products, including stability testing under ICH conditions. Instrumentation: Operate and maintain lab instruments such as HPLC, GC, UPLC, Karl Fischer (KF), dissolution apparatus, hardness tester, and disintegration apparatus. Data Management: Perform tests, record and report data as per approved procedures, and conduct data review, trending, and laboratory investigations (TrackWise system). Regulatory Compliance: Follow SOPs, cGMP guidelines, and regulatory procedures while ensuring adherence to internal methods and monographs. Team Collaboration: Assist other scientists to ensure timely project completion and provide support to lab personnel as required. Special Projects: Perform operational excellence activities, SOP revisions, and other assigned tasks.
Role Highlights
Perform stability and QC release testing on finished products. Conduct experiments from R&D to clinical and commercial release. Work with DEA-controlled substances following regulatory procedures. Ensure compliance with ICH and GMP regulations.
Qualifications
Education: Bachelor's degree in Analytical Chemistry, Pharmaceutics, or related field. Master's degree preferred. Experience: Minimum 3 years of industry experience in pharmaceutical product development. Expertise in analytical techniques including HPLC, GC, UPLC, FTIR, UV, KF, and wet chemistry. Skills: Strong knowledge of GMP and ICH regulations. Excellent written and verbal communication skills. Ability to interpret instructions in various formats (written, oral, diagram, schedule). Proficiency in data analysis and problem-solving under tight deadlines. Physical Requirements:Ability to sit, stand, walk regularly, and occasionally lift 0-15 pounds.
BCforward is currently seeking highly motivated Scientist - Quality Control & Analytical Product Development
Location: Somerset, NJDuration: 6+ months ContractJob Type: Contract
Anticipated Start Date: ASAP
(Please note this is the target date and is subject to change. BCforward will send official notice ahead of a confirmed start date.)
Job Type: Contract (40 hrs. a week)
Pay Rate: $39/hr
Please note that actual compensation may vary within this range due to factors such as location, experience, and job responsibilities, and does not encompass additional non-standard compensation (e.g., benefits, paid time off, per diem, etc.).
Key Responsibilities
Analytical Testing: Perform assays, dissolution, hardness tests, water content, content/blend uniformity, and related substances using wet chemistry as per compendial monographs. Laboratory Analysis: Conduct analytical testing of excipients, APIs, in-process, and finished pharmaceutical products, including stability testing under ICH conditions. Instrumentation: Operate and maintain lab instruments such as HPLC, GC, UPLC, Karl Fischer (KF), dissolution apparatus, hardness tester, and disintegration apparatus. Data Management: Perform tests, record and report data as per approved procedures, and conduct data review, trending, and laboratory investigations (TrackWise system). Regulatory Compliance: Follow SOPs, cGMP guidelines, and regulatory procedures while ensuring adherence to internal methods and monographs. Team Collaboration: Assist other scientists to ensure timely project completion and provide support to lab personnel as required. Special Projects: Perform operational excellence activities, SOP revisions, and other assigned tasks.
Role Highlights
Perform stability and QC release testing on finished products. Conduct experiments from R&D to clinical and commercial release. Work with DEA-controlled substances following regulatory procedures. Ensure compliance with ICH and GMP regulations.
Qualifications
Education: Bachelor's degree in Analytical Chemistry, Pharmaceutics, or related field. Master's degree preferred. Experience: Minimum 3 years of industry experience in pharmaceutical product development. Expertise in analytical techniques including HPLC, GC, UPLC, FTIR, UV, KF, and wet chemistry. Skills: Strong knowledge of GMP and ICH regulations. Excellent written and verbal communication skills. Ability to interpret instructions in various formats (written, oral, diagram, schedule). Proficiency in data analysis and problem-solving under tight deadlines. Physical Requirements:Ability to sit, stand, walk regularly, and occasionally lift 0-15 pounds.
Interested candidates please send resume in Word format Please reference job code 232251 when responding to this ad.
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