Quality Control Chemist - Pharmaceutical - 2816
Company Name:
Absolute Opportunities
Quality Control Chemist - Pharmaceutical - 2816
Role: Engineering or Related
Relocation Available: Yes
Industry: Engineering
Location: Missouri
Town / City: Union
Job Type: Permanent full-time
Job Description:
Contract manufacturer to the world's most trusted health and wellness brands looking for a Quality Control Chemist.
Primary responsibilities include performing all duties necessary as a QC Chemist under the general direction of the department supervisor. While performing duties, roles are flexible to improve how work is done, to streamline processes, and to meet deadlines. This position will report the Quality Laboratory Manager.
Job Functions:
Perform QC analysis of raw materials, in-process samples, and finished product and stability samples.
Conducts microbiological analysis on raw materials, in-process goods, and/or finished products and makes evaluation to determine conformance to specification.
Maintain data documentation in accordance with cGMP and company standards.
Interface with personnel from other companies/laboratories regarding testing discrepancies and method/instrument problems.
Maintain inventory of chemicals, apparatus, and equipment for analytical laboratory and satellite laboratories.
Maintain the analytical lab in accordance with GMP/Plant housekeeping procedures.
Experience:
Experience with reverse phase HPLC chromatography and Gas Chromatography. Experience with Agilent chromatography systems and Chemstation software is a plus.
Experience with AA and UV assays.
Experience troubleshooting the following laboratory equipment; HPLC, GC, AA, and UV.
Working knowledge of USP, EU compendia test methods for raw material testing.
Understanding of microbiological test methods and techniques.
Experience conducting OOS investigations.
Skills:
Excellent interpersonal skills.
Excellent oral and written communication skills.
Able to communicate with all levels in the organization.
Projects professional, responsive and positive image.
Detail oriented
Works independently with minimal supervision.
Qualifications:
Minimally, a BS degree in Chemistry OR BS degree in Biology or Microbiology with QC laboratory experience (including HPLC and GC) in a GMP environment
Three to five years' experience in a Quality Control Analytical laboratory working with HPLC, GC, AA, and UV instruments.
Experience performing Method Transfers
ASQC certification a positive.
Bottom Line Requirements:
1. BS degree in Chemistry, Biology, or Microbiology.
2. 3
years of QC laboratory experience (including HPLC and GC) in a GMP environment.
3. Experience performing Method Transfers.
4. ASQC certification is a plus.
5. Experience with Agilent chromatography systems and Chemstation software is a plus.Estimated Salary: $20 to $28 per hour based on qualifications.
Absolute Opportunities
Quality Control Chemist - Pharmaceutical - 2816
Role: Engineering or Related
Relocation Available: Yes
Industry: Engineering
Location: Missouri
Town / City: Union
Job Type: Permanent full-time
Job Description:
Contract manufacturer to the world's most trusted health and wellness brands looking for a Quality Control Chemist.
Primary responsibilities include performing all duties necessary as a QC Chemist under the general direction of the department supervisor. While performing duties, roles are flexible to improve how work is done, to streamline processes, and to meet deadlines. This position will report the Quality Laboratory Manager.
Job Functions:
Perform QC analysis of raw materials, in-process samples, and finished product and stability samples.
Conducts microbiological analysis on raw materials, in-process goods, and/or finished products and makes evaluation to determine conformance to specification.
Maintain data documentation in accordance with cGMP and company standards.
Interface with personnel from other companies/laboratories regarding testing discrepancies and method/instrument problems.
Maintain inventory of chemicals, apparatus, and equipment for analytical laboratory and satellite laboratories.
Maintain the analytical lab in accordance with GMP/Plant housekeeping procedures.
Experience:
Experience with reverse phase HPLC chromatography and Gas Chromatography. Experience with Agilent chromatography systems and Chemstation software is a plus.
Experience with AA and UV assays.
Experience troubleshooting the following laboratory equipment; HPLC, GC, AA, and UV.
Working knowledge of USP, EU compendia test methods for raw material testing.
Understanding of microbiological test methods and techniques.
Experience conducting OOS investigations.
Skills:
Excellent interpersonal skills.
Excellent oral and written communication skills.
Able to communicate with all levels in the organization.
Projects professional, responsive and positive image.
Detail oriented
Works independently with minimal supervision.
Qualifications:
Minimally, a BS degree in Chemistry OR BS degree in Biology or Microbiology with QC laboratory experience (including HPLC and GC) in a GMP environment
Three to five years' experience in a Quality Control Analytical laboratory working with HPLC, GC, AA, and UV instruments.
Experience performing Method Transfers
ASQC certification a positive.
Bottom Line Requirements:
1. BS degree in Chemistry, Biology, or Microbiology.
2. 3
years of QC laboratory experience (including HPLC and GC) in a GMP environment.
3. Experience performing Method Transfers.
4. ASQC certification is a plus.
5. Experience with Agilent chromatography systems and Chemstation software is a plus.Estimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
