QC Technician I at Cosette Pharmaceuticals Inc
Lincolnton, NC 28092, USA -
Full Time


Start Date

Immediate

Expiry Date

15 Nov, 25

Salary

0.0

Posted On

16 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Osha, Physical Testing, Access, Computer Skills, Waste, Excel

Industry

Pharmaceuticals

Description

Cosette Pharmaceuticals is a US based, diversified pharmaceutical company with a proven topicals and dermatology portfolio and a growing branded pharmaceuticals business. We are fully integrated, with a deep focus on internal R&D, high quality manufacturing standards and commercial sales excellence. We continue to diversify and expand through strategic partnerships, acquisitions and internal R&D.
Our highly experienced leadership team are busy writing the next, most ambitious chapter of our story. Building on a 100+ year heritage, their shared vision of innovation will leverage the expertise of more than 350+ team members, and infrastructure to create remarkable new opportunities for the patients and physicians we serve every day.
Cosette is headquartered in Bridgewater, NJ with 2 additional locations in the U.S. The South Plainfield, NJ office consists of an R&D Laboratory and other functional areas. The Lincolnton, NC site is a fully functioning, state of the art, manufacturing facility.

EDUCATION/TRAINING/WORK EXPERIENCE:

  • A High School Diploma and three years of experience at a GMP facility
  • Demonstrated computer skills, including all Microsoft Office applications (Excel, Access, Word, etc.)
  • Demonstrated knowledge of cGMPs, Safety, OSHA, and 21 CFR regulations and requirements
  • Demonstrated ability to multi-task while meeting established deadlines.
  • Proven record of compliance with regard to safety, GDPs, and general performance
  • Ability to work in a team environment.
  • Organizational skills and attention to details a must.
  • Willingness to be flexible.
  • Willingness to learn new tasks.

SPECIALIZED KNOWLEDGE AND SKILLS:

  • Log all samples into the applicable database assuring accuracy and completeness of data and any accompanying paperwork.
  • Understands requirements from SOPs and general GDP, for labeling and media sterilization. Understands chemical handling hazards and/or microbiological hazards and discards waste in compliance with all requirements.
  • Assists QC Analysts in physical testing to ensure timely release of laboratory results.
  • Order supplies when needed and with cost-effective means and pro-actively inventory the lab for future needs.

How To Apply:

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Responsibilities

BASIC PURPOSE:

Sample Log-in, tracking, and organization within sample room. Assist QC Analysts with routine work.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:

  • Maintain sample databases for stability, raw materials, finished products, and customer complaints in Chemistry and/or Microbiology and perform clerical work associated with sample tracking.
  • Label glassware and prepare initial sample into appropriate containers. Discard expired samples and solvents appropriately. Operate autoclave for sterilizing medias and decontaminating microbiological waste
  • Perform basic physical testing, including pH, viscosity, specific gravity, color determination, etc.
  • Maintain an inventory of lab supplies.
  • Other duties as assigned by management.
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