QC Laboratory Supervisor Microbiology
QC Laboratory Supervisor Microbiology
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Job Description
- Design and Startup Micro Lab on site.
- Supervise and coordinate resources to support routine and nonroutine sample testing.
- Effectively recruit the right people to support the laboratories activities and ensure that human resources are optimally utilized.
- Ensure lab spending are appropriate and within planned budgets.
- Ensure all testing are carried out in a timely and efficient manner to meet release leadtime and site metrics and Release of laboratory test results.
- Review and approve any method transfer or method qualification reports or equipment qualifications.
- Provide oversight on lab equipment calibration and maintenance program.
- Investigate and/ or provide guidance to resolve any deviation observed during lab testing or any other lab operations and ensure all CAPAs are implemented effectively.
- Develop and maintain environmental monitoring program and microbiological laboratory procedures.
- Lead validation of equipment and test methods for purified water.
- Lead test method transfer of microbiological method.
- Train laboratory team in operational tests and sampling methods.
- Participate and support audit preparation and audit responses including the development and implementation of programs to provide timely follow up on correctives and commitments.
- Participate in EHS Business Compliance cGMP and all other compliancerelated matters where applicable. Support CI initiatives and laboratory performance metrices.
- Provide technical support to laboratory personnel and provide guidance and training to all analysts to upgrade their technical competencies.
- Any other tasks as and when assigned by Supervisors.
Qualifications :
- Bachelor of Science majoring in Microbiology or related scientific degree.
- Master Degree in Microbiology or related scientific area.
- Minimum 5 years of pharmaceutical experience in an analytical testing environment within Quality department and with good knowledge of aseptic processes manipulation together with experience within a GMP environment and knowledge of current EU/FDA/ICH/IMB guidelines.
- Strong analytical mind with good problem solving and writing skills.
- Highly motivated and independent.
- Possess strong interpersonal and communication skills with ability to work within crossfunctional teams.
- Organized and resultoriented.
- Ability to work under tremendous pressures.
- Approachable with good leadership qualities.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
