Carlsbad company
Senior Quality Control Associate – Chemistry
Carlsbad company, Carlsbad, California, United States, 92002
Corporate Overview
Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.
Benefits and Pay Range
At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy:
Medical, Dental, and Vision Insurance
Company-Paid Life Insurance (1x Annual Salary)
Voluntary Life Insurance Options
Short-Term and Long-Term Disability Insurance
Flexible Spending Account (FSA)Health Savings Account (HSA)
401(k) Retirement Plan with Company Matching
14 Days of Paid Time Off (PTO)
10 Paid Holidays Annually
The pay range for this position is $130,000 - $140,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.
Position Overview The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product and stability test samples. Further support services includes processing and testing of environmental monitoring and raw material samples. QC personnel are responsible for compliance to QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. This role is an on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Responsibilities and Duties Management of incoming samples utilizing a laboratory information system (LIMS) or other means.
Perform detailed chemical analysis of samples from production, routine monitoring, stability and validation or qualification studies using compendial and non-compendial methods
Utilize advanced instruments such as HPLC/UHPLC, SoloVPE, Maurice (cIEF and SDS Page), FTIR and UV/Vis Spectrophotometers
Author protocols and reports including but not limited to, method qualification, method verification, method validation and method suitability.
Apply and adhere to data integrity principals to sample handling and analysis
Manage deviation/OOS investigations and implement CAPAs and change controls per GMP requirements
Author and revise QC related SOPs as required
Interface with product Sponsors on QC related inquiries.
Participate in the review and approval of Manufacturing Batch Records for QC related activities
Execute analytical method transfer activities, including product-specific test methods
Train junior personnel in appropriate laboratory and safety procedures
Execute Installation and Operational Qualification of analytical instrumentation where applicable
Directly contributes to daily laboratory operations for QC Chemistry in full compliance with applicable SOPs and safety guidelines
Requirements and Qualifications Undergraduate degree (B.A. or B.S.) in a Life Science discipline
A minimum of 7 years' experience in a GMP-compliant Quality Control function within the medical device and/or biopharmaceutical fields
A high level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction
Analytical experience in the following methodologies: Buffer Characterization (pH, conductivity, osmolality), Concentration (UV/Vis and/or Fluorescence), Chromatography (HPLC, Electrophoresis)
The ability to work effectively within cross functional teams comprised of Manufacturing, Tech Transfer, Quality Assurance, and Senior Management
An affinity for precise and detailed documentation skills.
The ability to effectively influence and contribute to a dynamic and fast-paced work environment
A strong work ethic and a high level of accountability
Strong oral and written communication and listening skills
Excellent Problem-solving skills
Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
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Position Overview The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product and stability test samples. Further support services includes processing and testing of environmental monitoring and raw material samples. QC personnel are responsible for compliance to QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. This role is an on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Responsibilities and Duties Management of incoming samples utilizing a laboratory information system (LIMS) or other means.
Perform detailed chemical analysis of samples from production, routine monitoring, stability and validation or qualification studies using compendial and non-compendial methods
Utilize advanced instruments such as HPLC/UHPLC, SoloVPE, Maurice (cIEF and SDS Page), FTIR and UV/Vis Spectrophotometers
Author protocols and reports including but not limited to, method qualification, method verification, method validation and method suitability.
Apply and adhere to data integrity principals to sample handling and analysis
Manage deviation/OOS investigations and implement CAPAs and change controls per GMP requirements
Author and revise QC related SOPs as required
Interface with product Sponsors on QC related inquiries.
Participate in the review and approval of Manufacturing Batch Records for QC related activities
Execute analytical method transfer activities, including product-specific test methods
Train junior personnel in appropriate laboratory and safety procedures
Execute Installation and Operational Qualification of analytical instrumentation where applicable
Directly contributes to daily laboratory operations for QC Chemistry in full compliance with applicable SOPs and safety guidelines
Requirements and Qualifications Undergraduate degree (B.A. or B.S.) in a Life Science discipline
A minimum of 7 years' experience in a GMP-compliant Quality Control function within the medical device and/or biopharmaceutical fields
A high level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction
Analytical experience in the following methodologies: Buffer Characterization (pH, conductivity, osmolality), Concentration (UV/Vis and/or Fluorescence), Chromatography (HPLC, Electrophoresis)
The ability to work effectively within cross functional teams comprised of Manufacturing, Tech Transfer, Quality Assurance, and Senior Management
An affinity for precise and detailed documentation skills.
The ability to effectively influence and contribute to a dynamic and fast-paced work environment
A strong work ethic and a high level of accountability
Strong oral and written communication and listening skills
Excellent Problem-solving skills
Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
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