Production Compliance Specialist
- $61,000 - $70,000
- Covina, CA
Come join a leading global pharmaceutical manufacturer!! With us you can influence change and make a difference.
A bit about us:
A leading global manufacturer of pharmaceuticals
Why join us?
We have a caring, family culture which ensures employees feel supported in their personal and professional lives. We work through challenges together and provide a working environment where people feel valued and where they can learn and grow within our business.
Job Details
We are seeking a highly motivated and experienced Quality Compliance Specialist to join our team in the scientific industry. The ideal candidate will have a strong background in pharmaceuticals, cGMP, aseptic techniques, and equipment. As a Quality Compliance Specialist, you will be responsible for ensuring that all production processes meet regulatory and quality standards. This is a permanent position that offers an exciting opportunity to work in a dynamic and fast-paced environment.
Responsibilities:
Qualifications:
If you are a self-starter who thrives in a challenging and fast-paced environment, we encourage you to apply for this exciting opportunity. We offer a competitive salary and benefits package, as well as opportunities for career growth and development.
Responsibilities:
- Monitor and maintain compliance with cGMP regulations and other regulatory requirements
- Conduct investigations into deviations and non-conformances, and develop corrective and preventive actions
- Review and approve batch records, packaging records, and other production documents
- Provide guidance and oversight to production personnel to ensure compliance with quality standards
- Participate in the development and implementation of quality improvement initiatives
- Conduct internal audits to ensure compliance with company policies and procedures
- Support external audits and regulatory inspections
- Perform risk assessments and develop risk mitigation strategies
- Maintain accurate and complete records of compliance activities
Qualifications:
- Bachelor's degree in a scientific discipline
- 2+ years of experience in the pharmaceutical industry, with a focus on quality compliance
- Knowledge of cGMP regulations and other regulatory requirements
- Experience with aseptic techniques and equipment
- Strong analytical and problem-solving skills
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Experience in a supervisory or leadership role is a plus
- Knowledge of production processes and batch record review is preferred
If you are a self-starter who thrives in a challenging and fast-paced environment, we encourage you to apply for this exciting opportunity. We offer a competitive salary and benefits package, as well as opportunities for career growth and development.
Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.