Associate Chemist

Associate Chemist


Job ID: 9671151

Philadelphia, NJ, US

Scientific

Associate Degree

Full Time, Direct Hire

Entry Level

On-site

Biotechnology/Pharmaceuticals

First Shift (Day)

Philadelphia, NJ, US

Entry Level

Full Time, Direct Hire

Biotechnology/Pharmaceuticals

On-site

Scientific

Associate Degree

First Shift (Day)

Job details

Laboratory Technician- Permanent Position
1st shift and 2nd shift available- Monday to Friday
Job Summary:
In this role, you will ensure that cGMP (current Good Manufacturing Practices) standards are upheld to guarantee process and product quality. You will work closely with various teams to maintain quality assurance across all stages of production and ensure compliance with company policies, regulatory requirements, and safety standards.

Essential Duties and Responsibilities:

  • Assist in maintaining and updating Master Batch Record documentation, including new, revised, and obsolete records.

  • Review Production Batch Record documentation to ensure accurate product release.

  • Assist with investigations to identify and resolve quality issues.

  • Ensure adherence to company policies, regulatory requirements, quality specifications, safety standards, and sanitation practices.

  • Conduct routine audits of production processes, perform quality reviews of documentation and production processes to ensure compliance with cGMP standards.

  • Collaborate with teams to ensure continuous improvement in maintaining cGMP standards across the organization.

Required Education and Experience:

  • Bachelor’s Degree in Biological Science, Chemistry, Biomedical Engineering, or a related field or relevant work experience.

  • Ability to work with chemicals used in compound preparation while following all required safety protocols. Ability to wear required personal protective equipment.

  • Strong understanding of basic principles, policies, and procedures related to compounding.

Preferred but not required skills.

  • Experience in a pharmaceutical/cosmetic manufacturing environment or a similar role

  • Familiarity with GxP, FDA, ICH, and OSHA requirements

  • Proficient in Minitab, Excel, and other relevant software applications

Competencies:

  • Excellent punctuality and low absenteeism record. Strong communication proficiency, both verbal and written. Problem-solving and analytical skills to identify and address quality issues. Commitment to maintaining high-quality standards and ensuring consistent product quality.

9671151

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