Company

ActalentSee more

addressAddressSummerville, SC
type Form of workFull-Time
CategoryManufacturing

Job description

Job Description

First shift position with a chemical manufacturing company. We are looking for a candidate with working experience in Chemistry or a related life science field. If you are interested in pivoting from benchwork to a position within QA, please email your resume to Kiley at klamagdeleine@actalentservices.com! to set up an intro call.

Description:

The Quality Assurance Technician is responsible for the execution and support of all tasks related to Operational and System Quality Assurance as defined by cGMP for all regulated materials in the facility.

Shift:

M-F / Day shift; 8AM - 4PM. Hours per week: 40.

Day to Day duties:

- Perform Batch record review and data trending

- Perform Audit Trail Review for regulated Finished Products

- Preform Audit Trail Review for Raw Materials

- Preform Laboratory Record Review

- Review Out of Specification process (OOS) and Out of Trend process (OOT)

- Maintain the validation and calibration master plans

- Review and approve validation protocols and reports

- Write, review and update procedures

- Collect data for Annual Product Review

- Assists with internal and external audits if necessary

- Assists with non-conformance investigations

- Assists with Customer Questionnaires

- Performs all other QA related tasks as assigned by the Sr. Manager QA and NA cGMP

Skills:

Quality assurance, Gmp, Chemistry, Batch record, Capa, Audit, Batch record review, Document control, Laboratory

Additional Skills & Qualifications:

• BS in Chemistry or related field or equivalent experience preferred.

• Experience working in a laboratory environment required.

• Knowledge of cGMP for pharmaceuticals highly desired.

• Familiarity with various laboratory analysis techniques used within lab (GC, GC-MS, XRF, MP/BP, FT-IR, RI, Colorimetry, Polarimetry, pH, etc.)

• Thorough understanding of cGMPs for food and pharma.

• Familiarity with the Bushy Park process flow.

• Excellent organizational skills, analytical thinking ability, and effective communication skills are essential.

• Strong Time Management skills

• The ability to work as a team player in the laboratory while maintaining a strong rapport with plant operations.

• Possess a thorough understanding of safety policies and procedures.

• Proficient in Microsoft Office, Chromeleon and SAP.

Safety/Regulatory Training Requirements:

HACCP, Food and Pharma cGMP, PPE, Chemical Hygiene

Experience Level:

Entry Level

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.

Refer code: 7750013. Actalent - The previous day - 2024-01-07 05:12

Actalent

Summerville, SC
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