Job Description

　　Location/Division Specific Information

　　St. Louis, MO

　　Discover Impactful Work:

　　Successfully lead departmental manufacturing resources in order to deliver on customer commitments and expectations. Ensure right the first time and on time delivery of mammalian cell culture processes and protein purification processes to support clinical and commercial biologics manufacturing. Demands are to be met in accordance with established safety, quality, efficiency and regulatory standards. Lead all aspects of all manufacturing resources including personnel and equipment. Operate cross functionally and collaborate with peers both within and outside of department. Successfully drive focused performance management and talent development of direct and in-direct reports. Demonstrating proactive leadership inside of the department and strategic delivery of company goals and a continuous improvement approach is also an expectation.

　　A day in the Life:

　　Lead day to day operations to ensure departmental commitments and deliverables are achieved to meet company objectives. This involves resource oversight, planning, delegation, prioritization, collaboration, etc. for Manufacturing groups.

　　Maintain open communication via one-on-one and team meetings, and assure supervisory files are kept up to date.

　　Encourage and lead all aspects of a culture of compliance regarding Safety, Environmental, Quality standards as required by cGMPs, Health Authority regulations, government agencies, and company standards / policies. Support all site audits and inspections.

　　Ensure adequate manufacturing resources are dedicated to correcting important or critical issues

　　Serve as a leader on departmental and site teams to improve and challenge processes, solve problems, initiate improvements, establish procedures, transfer new products or technologies, implement projects, etc.

　　Responsible for working with the Senior Manager to mature area systems on an annual basis

　　Conduct hiring, coordinate training, prepare and communicate staff evaluations. Develop a team that is highly respected, engaged and actively develop and train high potential candidates for the next generation of leaders.

　　Be a role model. Exude optimism. Support company direction and officers. Be a supporter and an asset to your peers. Be a representative for Manufacturing on site and back up / delegate for the backup for the area Senior Manager as the need arises.

　　Select, develop and evaluate staff to ensure the efficient operation of the function. Work with and advise staff on administrative policies and procedures.

　　Keys to Success:

　　Education

　　Bachelor’s degree requiredExperience

　　5-7 years of industry experience, preferably in a cGMP environment

　　3-7 years of management (leadership and talent development) experience

　　Demonstrated success with continuous improvement and a dedication to craftsmanship and putting quality first.

　　Knowledge, Skills, Abilities

　　Understanding of production processes and the biopharma production environment

　　Excellent understanding of cGMP and other regulatory requirements in the operation of cleanrooms

　　Understanding of cGMP quality systems (e.g. change control, deviations, investigations, risk assessments, driving GDP within all documentation and records).

　　Strong leadership skills to influence and build effective teams, gain agreement via collaboration, and handle difficult situations with tact and diplomacy.

　　Mechanical and technical ability/proficiency

　　Analytical problem-solving skills.

　　Excellent planning and organizational skills and the ability to efficiently handle multiple tasks, issues, projects.

　　Unquestionable integrity, dedication to EH&S and accountable when making sure teams follow regulations and procedures.

　　Organized, efficient, and results oriented

　　Good people coaching and development skills

　　Expert in oral and written communication (verbal and written in English), as well as social skills.

　　Computer literate with Microsoft Office tools, including report writing and graphing.

　　Quality and/or Financial software (SAP, eDMS, Trackwise, LIMS, etc) skills a plus.

　　Physical Requirements / Work Environment

　　Be willing to wear a full gowning suit which includes: bodysuit, gloves, hair & beard nets, face covers, and safety glasses. (These items are prohibited: makeup, jewelry, nail polish, cologne / perfume, scented lotions or hair care products, etc.) Able to meet clean room gowning requirements, including wearing Tyvek, Nitrile, and/or Latex gloves

　　Ability to lift minimum of 25 lbs independently

　　Ability to stand for 80% of shift

　　Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.