Supervisor, Quality Control

DPT Laboratories, Ltd.

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

• Access

• Providing high quality trusted medicines regardless of geography or circumstance;

• Leadership

• Advancing sustainable operations and innovative solutions to improve patient health; and

• Partnership

• Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here's how the Supervisor, Quality Control role will make an impact:

• Supervise the chemistry laboratories in a cGMP Chemistry Laboratory environment.

• Provide technical expertise and guidance to group.

• Mentor and coach staff personnel assigned to the department, facilitating and assisting in their growth within DPT.

• Promote the technical and professional development of direct reports.

• Work under minimal supervision - work is only reviewed upon completion for adequacy in meeting objectives.

• Ensure that lab personnel remain current and trained on all internal SOPs and follow cGMP practices at the plant. Provide training as necessary.

• Develop goals and objectives for direct reports to include the review and evaluation of job performance of direct reports.

• Provide daily guidance to the analysts in their various work activities.

• Investigate product anomalies and failures.

• Follow all company policies and all current FDA guidelines and any other applicable regulations.

• Promote cleanliness of the laboratory and possess a working knowledge of all laboratory equipment.

• Implement change control requirements. Write, update, review, and approve pertinent SOPs and analytical methods.

• Develop strong inter-departmental relationships.

• Work closely with internal and external departments to ensure the efficient progress of projects.

• Be able to interact with Clients in a professional manner.

• Within area of responsibility, understand and comply with all safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs as well as applicable federal, state, and local regulations.

• Perform other duties as assigned.

The minimum qualifications for this role are:

• Bachelor's of Science degree (B.S.) from a four-year College or university is required. Master's degree is preferred.

• Minimum 6 - 9 years of quality control/laboratory, and/or analytical testing experience within a pharmaceutical and/or cGMP environment is required with a Bachelor's degree. 4 - 7 years quality control/laboratory, and/or analytical testing experience within a pharmaceutical and/or cGMP environment is required with a Master's degree.

• Minimum 3-5 years in a leadership and/or supervisory capacity is required with a Bachelor's degree minimum 1-2 years in a leadership and/or supervisory capacity is required with a Master's degree.

• Requires skills necessary to analyze and interpret data.

• Requires thoroughness and a practical application of chemical knowledge.

• Demonstrates leadership skills.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.