QC weekend Team lead

Oxoid Remel Microbiology

Lenexa (KS)

On-site

USD 65,000 - 85,000

Full time

14 days+
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Job summary

Oxoid Remel Microbiology, part of Thermo Fisher lineage and now under Astorg, seeks a Quality Control weekend Team Lead in Lenexa, KS. You will oversee weekend QC lab operations, assign duties, and ensure compliance with FDA/ISO standards while training staff.

The role requires a 4-year biology degree (microbiology preferred), prior lab leadership experience, and strong English communication. Weekend shifts from Friday to Monday may adjust with business needs.

Qualifications

  • Bachelor's degree in biological sciences (microbiology preferred).
  • 1–3 years in a lab lead/supervisory role with direct reports.
  • 4 years microbiology lab experience preferred.
  • Familiarity with FDA regulations for medical devices and USP/CLSI.
  • Strong English verbal and written communication skills.

Responsibilities

  • Oversee weekend operation of the Quality Control Laboratory.
  • Manage weekend team performance and training.
  • Provide lab bench coverage during absences.
  • Maintain SOPs in Master Control per FDA/ISO regulations.
  • Ensure GMP/GLP compliance and safety.

Skills

Time management
Team leadership
English communication
Adaptability
Attention to detail

Education

Bachelor's in Biological Sciences

Tools

SAP
Microsoft Office

Job description

Workday ID: R-01357305

Joining our team, you’ll play an active part in helping to deliver meaningful impact. At Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, we play a crucial role in accurate identification and targeted treatment for diseases, ensuring food and beverage safety, and supporting pharmaceutical manufacturing integrity. Our products and services are designed to meet the highest standards of quality and performance, helping our customers achieve their objectives efficiently and effectively.

Job Title: Quality Control weekend Team Lead

Reports To: Quality Control Supervisor

Group/Division: SDG/MBD

Career Band: Band 5

Position Location: Lenexa Kansas

Number of Direct Reports 3, potential for more

Day/Shift (if applicable): Friday to Monday, could possible change based on business needs.

FLSA Status (Exempt/Non-Exempt): Exempt

About the Role

Oversee the weekend operation of the Quality Control Laboratory. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines.

Key Responsibilities
  • Assist Quality Control Supervisor in daily laboratory operations and assign job duties to Quality Control staff as needed.
  • Manage weekend team to include performance management and goal setting.
  • Provide lab bench coverage during absences.
  • Oversee personnel issues within the department.
  • Develop and train new employees, maintaining consistency in training/development of existing personnel.
  • Create, update and maintain SOP’s for lab procedures in Master control in accordance with FDA and ISO regulations as assigned.
  • Initiate Issue Review’s and implement root cause counter measures as directed.
  • Initiate IN’s for the Out of specifications products to submit to QA.
  • Work closely with other Quality departments to provide up to date product information.
  • Exercise and monitor GMP and GLP compliance in work environment.
  • Lead and facilitate continuous improvement program within department.
  • Understand and exercise all safety requirements and procedures.
  • Work closely with a team in a fast-paced laboratory setting.
  • Responsible for achieving department goals.
  • Maintain consistent training in Master Control.
  • Understand and exercise all safety requirements and procedures.
  • Support all company policies.
  • Performs other duties as assigned.
Minimum Requirements & Qualifications
  • Possess a 4-year degree in the biological sciences – microbiology preferred
  • Preferred 1-3 years in a lab lead/supervisory roll with direct reports
  • 4 years microbiology lab experience preferred
  • Familiarity with plate and tube media, bacterial and fungal culturing
  • Familiarity with FDA regulations for medical devices.
  • Understanding of USP and CLSI requirements.
  • Possess the ability to manage many tasks and in an organized fashion.
  • Possess computer skills - experience in Microsoft Office to include Word, Excel and PowerPoint programs. Experience working in SAP
  • Listen to, and follow, written and verbal instructions.
  • Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
  • Must be available to adjust work shift when needed.
  • Self-motivated, highly responsible and possess a good positive teamwork spirit.
  • Excellent verbal and written skills in English.

Non-Negotiable Hiring Criteria: (Bullet 3-5 key quantifiable skills or position requirements that the candidate must have to be considered for this position.)

  • Candidate must be a good time manager.
  • Candidate must be willing to put in overtime when needed to complete tasks.
  • Candidate must be a good team player/participant on teams.
  • Candidate must have a high sense of responsibility and Positive attitude.
  • Candidate must possess critical thinking skills.

This position has not been approved for Relocation Assistance.

This is an exciting time to join us as we continue to build on more than 100 years of microbiology excellence. With a broad portfolio of instruments, services, and global resources, we’re steadfast in our commitment to helping you succeed. Together, we can cultivate a thriving microbiology culture that supports you today, tomorrow, and for life. Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, is now under the ownership of Astorg, a leading private equity firm with deep healthcare sector expertise and proven track record in diagnostics. With the continuity of trusted brands, established expertise and a long-standing reputation in microbiology, we’re looking for talented people to join us as we enter our next chapter of growth. Come and be part of what’s next for our company.

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