Quality Control Manager

• Full-time, permanent position
• Gulfport, Mississippi, USA
• Enjoy coastal living
  
  

Are you a seasoned Quality Control Manager? Are you looking for an opportunity to join a team of experienced professionals and work for a stable and quality-focused company?

If this sounds like you, we want to hear from you!

We’re Raise, and we’ve joined forces with our client, a world-leading manufacturer of liquid antacids. Their high volume capacity and superior quality control make them the first choice for discerning private-label brands. They offer state-of-the-art technology, unparalleled service, economical pricing, and a professional team that is dedicated to servicing over-the-counter and personal health needs.

What You’ll Be Doing

As the new Quality Control Manager, you’ll be responsible for managing laboratory personnel and maintaining the laboratory to ensure all products and procedures meet the requirements of 21CFR210, 21CFR211, Regulatory Agencies, and customer expectations.

Responsibilities

• Maintain the laboratory quality management system to ensure compliance with cGMP
• Audit the Quality Control Laboratory to ensure compliance to SOP’s
• Investigate, assess, and troubleshoot test and/or equipment problems
• Review Out-of-trend/Out-of-specification results and participate in investigations to determine root cause and CAPA
• Ensure analytical equipment is calibrated and well maintained at all times
• Ensure that laboratory personnel training requirements are met and that training records are current
• Interview, hire, and train new staff
• Provide constructive feedback and retraining as needed
• Handles discipline of employees in accordance with company policy
• Maintain the laboratory quality management system to ensure compliance with cGMP
• Establish product test methods and specifications. This includes raw materials, in-process product, finished products and stability samples
• Audit the Quality Control Laboratory to ensure compliance to SOP’s
• Maintain appropriate laboratory inventory to ensure timely release of materials
• Participate in method qualifications, validations, and transfers
  
  

The successful candidate will be a strong leader and manager with a thorough understanding of FDA, cGMP, SOPs quality control & lab standards. They are solution-oriented and possess exceptional accuracy and attention to detail. Committed to achieving deadlines in a fast-paced environment, they maintain a strong focus on delivering high-quality work and products.

The Details

This is a full-time, permanent position located in the vibrant city of Gulfport, Mississippi, where you can enjoy the charm of coastal living. Gulfport offers a diverse range of activities and attractions for everyone. You will work from the Gulfport facility, Monday through Friday. Relocation assistance is available on a case-by-case basis. In addition to a competitive base salary starting at $100,000 per year (commensurate with experience), you will also a benefits package and vacation time.

Qualifications

• B.S. in Chemistry, Biology, or a related discipline
• 10 years of management experience in a pharmaceutical laboratory setting
• Pharmaceutical experience required
• Expert knowledge and understanding of quality control, SOPs, cGMPs, OSHA, and FDA policies and regulations
• Experience in computer software, such as Microsoft applications
• Excellent verbal and written communication skills in English
• Excellent management and teamwork skills
• Excellent organizational skills and attention to detail
• Excellent time management skills with a proven ability to meet deadlines
• Ability to function well in a high-paced and at times stressful environment
• Ability to understand and follow all Standard Operating Procedures and current Good Manufacturing Practices provided by the Company
• Knowledge and control of analytical equipment including calibration and maintenance
• Understanding of quality systems including change control, deviations and CAPAs
• Ability to handle multiple tasks concurrently and complete them in a timely manner
  
  

Your Application

We value diversity and inclusion and encourage all qualified people to apply; however, only those selected for an interview will be contacted.

Looking for meaningful work? We can help

Raise is an established hiring firm with over 65 years of experience. We believe strongly in making the world a better place through work, which is why we’re a certified B Corporation and donate 10% of our profits to charity.

We strive to build teams that reflect the diversity of the communities we work in. We encourage all qualified applicants to apply, including people from traditionally underrepresented groups such as women, visible minorities, Indigenous peoples, people identifying as LGBTQ2SI, veterans, and people with visible/nonvisible disabilities.

We have a dedicated webpage for accommodations where you can learn more about what we offer, and request accommodation: https://raise.jobs/accommodations/

In order to submit candidates for roles, our clients will sometimes require personal information to confirm the identity of applicants and their legal status to work. Raise will never ask you for personal or banking information unless you have been selected for a job. If you are ever unsure about the legitimacy of this or another job posting by Raise (or have any other questions), please contact us at 1 800-567-9675 or hello@raiserecruiting.com

#IMSMB