Associate Scientist II - Quality Control, Microbiology

Catalent Pharma Solutions; Alabama; On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

401K match

Medical, dental and vision benefits

PTO + holidays

Job summary

Catalent Pharma Solutions in Madison, WI is seeking an Associate Scientist II - Quality Control, Microbiology for an on-site, Sunday-Tuesday 6am-6pm schedule. The role focuses on cGMP QC testing and data documentation in a fast-growing biologics setting.

The candidate will work with SOPs, Trackwise, and LIMS, performing maintenance and data entry while contributing to quality control operations within a diverse, patient-centered team.

Qualifications

• Bachelor’s degree in biology, biotechnology, chemistry or related field with a minimum of 1 year of industry experience.
• Associate degree in biology, biotechnology, chemistry or related field with a minimum of 4 years of industry experience.
• High school diploma or equivalent with a minimum of 6 years of industry experience.
• Familiarity with cGMP, GDP, or GLP knowledge; SOP experience; general lab equipment experience including micropipettes.

Responsibilities

• Executes and documents cGMP Quality Control testing with minimal supervision.
• Operates basic to moderately complex cGMP QC equipment with supervision.
• Performs self-review of analytical data for accuracy against SOP.
• Enters data into LIMS or lab reports.
• Maintains general lab housekeeping following 5S standards.
• Initiates records in Trackwise.
• Completes routine and preventive maintenance on equipment.
• Participates in team meetings and training sessions.
• Other duties as assigned.

Skills

Lab techniques

GDP/GMP knowledge

SOP adherence

Micropipette use

Education

Bachelor’s Degree in Biology/Biotech/Chemistry

Associate Degree in Biology/Biotech/Chemistry

High School Diploma with 6+ years experience

Tools

LIMS

Trackwise

Analytical instruments

Job description

Associate Scientist II - Quality Control, Microbiology

Position Summary:

• Work Schedule: Sunday - Tuesday 6am-6pm

• 100% on-site

Working for Catalent Biologics is an opportunity to join an entrepreneurial team. Catalent Biologics is making significant investments in people and capabilities. This is a unique opening to join a small, fast-growing business, backed by a global public company. People joining our team will have the opportunity for career development as our business continues to grow and expand. Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart, and lung diseases as well as Alzheimer’s.

Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist II - Quality Control, Microbiology.

The Role:

• Executes and properly documents cGMP Quality Control testing with minimal supervision.
• Independently operates basic cGMP Quality Control equipment and moderately complex cGMP Quality Control equipment with supervision.
• Performs self-review of analytical data for accuracy and consistency with SOP.
• Enters data into Laboratory Information Management System (LIMS) or laboratory reports.
• Performs general lab housekeeping in adherence to 5S standards.
• Initiates records in Trackwise.
• Accurately completes routine and preventive maintenance on basic to moderately complex equipment.
• Actively participates in team meetings and/or training sessions.
• Other duties as assigned.

The Candidate:

• Bachelor’s Degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 1 year of industry experience.
• Associate Degree in Biology, Biotechnology, Chemistry or related life sciences field with a minimum of 4 years of industry experience.
• High School Diploma or equivalent with a minimum of 6 years of industry experience.
• Preferred:
  • Basic understanding of analytical chemistry and simple lab equipment.
  • Familiarity with clean room procedure, aseptic technique, and general lab equipment experience.
  • cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge.
  • Experience following standard operating procedures (SOP).
• General laboratory equipment experience, including micropipettes.

Why you should join Catalent:

• Defined career path and annual performance review and feedback process
• Diverse, inclusive culture
• Positive working environment focusing on continually improving processes to remain innovative
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
• 152 hours of PTO + 8 paid holidays
• Generous 401K match
• Medical, dental and vision benefits effective day one of employment
• Tuition Reimbursement- Let us help you finish your degree or start a new degree!

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

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