Position Title: Quality Control Manager, Pharmaceutical
Position Location: Southwest Avenue St. Louis, MO, USA
Relocation offered: Not Applicable
Pay Range / Details / Bonus: Base of $85k - $90k + bonus
Role Type (Perm/Temp) : Permanent
Interview Process: 3 phone interviews, one video then offer
Does client do background checks: No
Additional Info on client / Notes: Great culture. Very invested in their teams’ success. Quick interview process with NO HR involvement
Job Description
We are looking for a detail-oriented Quality Control Manager to ensure the manufacturing production lines run smoothly and generate a consistently suitable output of products that meet quality and efficiency standards..
Responsibilities:
* Provide NetSuite assistance and support to existing clients and new clients.
* Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams.
* Devising ways to improve the manufacturing process to ensure higher-quality goods.
* Devising, improving, and reviewing new specifications and procedures for products or processes, and training staff to use them.
* Setting the requirements for raw materials from suppliers and monitoring their compliance.
* Supervising inspectors, technicians, and other staff members and providing guidance.
* Ensuring legal obligations are followed and ensuring compliance with regulatory bodies and with health and safety guidelines.
* Overseeing product development procedures to identify any deviations from quality standards.
* Inspecting the final output, comparing it to the requirements, and approving or rejecting the final products.
* Keeping accurate documentation and performing statistical analysis.
* Gaining feedback from the clients, attending meetings, submitting reports, and assisting external auditors and inspectors.
Requirements:
* A bachelor's degree in science or business-based programs.
* At least 5 year Supervisory / management experience under Pharmaceutical industry
* Strong knowledge of cGMP and FDA regulations for method development, validation, and transfer
* Previous experience in production or manufacturing under pharmaceutical industry.
* Experience in business administration may be advantageous.
* Strong attention to detail, observation, organizational, and leadership skills.
* In-depth knowledge of quality control procedures and legal standards.
* Strong knowledge of mathematics, data analysis, and statistical methods.
* Excellent communication and listening skills
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Apply Now
To apply, the interested candidate may submit his/her updated English resume with photo by clicking the "apply now" button below.
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