Planet Pharma
This range is provided by Planet Pharma. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $38.00/hr - $42.00/hr
CONTRACT : 10-month extendable
MUST HAVES:
B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent
Experience in method transfer/implementation; understanding of method lifecycle management
Job Overview :
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.
Key Responsibilities
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep; review data timely and qualify as a data reviewer.
Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
Contribute to updating controlled documents (SOPs, work instructions, test methods).
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
Participate in continuous improvement initiatives and cross-functional collaboration.
Support regulatory submissions, inspection readiness, and audits.
Qualifications
B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
Experience in method transfer/implementation; understanding of method lifecycle management preferred.
Strong technical writing, data analysis, problem-solving, and organizational skills.
Excellent communication and teamwork; proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred.
Seniority Level Associate
Employment type Full-time
Job Function Quality Assurance, Research, and Science
Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
Benefits Medical insurance Vision insurance 401(k)
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Base pay range $38.00/hr - $42.00/hr
CONTRACT : 10-month extendable
MUST HAVES:
B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent
Experience in method transfer/implementation; understanding of method lifecycle management
Job Overview :
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.
Key Responsibilities
Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs.
Support weekend lab operations and maintain training records.
Assist in lab equipment and inventory maintenance, including reagent and sample prep; review data timely and qualify as a data reviewer.
Perform operational assignments (raw material processes, environmental monitoring, in-process testing).
Contribute to updating controlled documents (SOPs, work instructions, test methods).
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH).
Participate in continuous improvement initiatives and cross-functional collaboration.
Support regulatory submissions, inspection readiness, and audits.
Qualifications
B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent.
Experience in method transfer/implementation; understanding of method lifecycle management preferred.
Strong technical writing, data analysis, problem-solving, and organizational skills.
Excellent communication and teamwork; proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred.
Seniority Level Associate
Employment type Full-time
Job Function Quality Assurance, Research, and Science
Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
Benefits Medical insurance Vision insurance 401(k)
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