Quality Control Scientist - Switch4 LLC
Danbury, CT 06810
About the Job
Job Title: Quality Control Scientist
Location: Danbury, CT
Job-Type: Full Time/Permanent
Working Hours: 12:30pm to 9pm, Tuesday to Saturday
Job Summary:
Provides general support to maintain quality control systems within the company. Ensures that performance and products conform to established company and regulatory standards. Analyzes finished formulations, raw materials, in process materials, or stability samples by HPLC/GC, in support of the company's quality program. Interprets and evaluates the analyses in terms of accuracy and precision and recommends corrective action where necessary. Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.
Essential duties and key job responsibilities and essential functions.
Minimum qualifications to perform the job; specific skills, education, knowledge and job experience necessary to perform essential duties; physical requirements for job if any.
Skills and Certifications:
Location: Danbury, CT
Job-Type: Full Time/Permanent
Working Hours: 12:30pm to 9pm, Tuesday to Saturday
Job Summary:
Provides general support to maintain quality control systems within the company. Ensures that performance and products conform to established company and regulatory standards. Analyzes finished formulations, raw materials, in process materials, or stability samples by HPLC/GC, in support of the company's quality program. Interprets and evaluates the analyses in terms of accuracy and precision and recommends corrective action where necessary. Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation.
Essential duties and key job responsibilities and essential functions.
- Conduct routine and non-routine HPLC/GC analysis of raw materials, in process, and finished formulations according to standard operating procedures.
- Perform chemical analyses of product to ensure stability.
- Compile data for documentation of test procedures that may include microbiological and/or chemical assays, stability program testing and formulation studies.
- Calibrate and maintain lab equipment.
- Participate in the preparation of investigations, summaries and reports.
- May assist in developing testing methods.
- Review data obtained for compliance to specifications and report abnormalities.
- Revise and update standard operating procedures as needed.
- May perform special projects on analytical and instrument problem solving.
- Applies knowledge of good manufacturing practices, good laboratory practices and good record keeping practices on a daily basis.
- Follows written test methods and protocols.
- Process data, report data and prepare tables and graphs for the completed testing. Identify problems, e.g. out of trend data. Professional interactions are primarily within the QC organization.
- Responsible for observing all Company, Health, Safety and Environmental guidelines.
Minimum qualifications to perform the job; specific skills, education, knowledge and job experience necessary to perform essential duties; physical requirements for job if any.
- BS Degree in a scientific discipline with 2 to 4 years' experience or MS or MBA 1 to 3 years or related experience or an equivalent combination of training and experience
- At least 4 years' experience in a laboratory setting, preferably in pharma
- 3-5 years' experience in quality control systems
- Good written communication skills
- Understanding of GMPs and regulatory guidelines as they relate to the pharmaceutical products preferred
- Good interpersonal skills
- Access, Excel, Word and Power Point skills.
Skills and Certifications:
- Empower
- HPLC
Raw Materials - Finished Products
- Pharmaceutical Experience
Source : Switch4 LLC