Top 2791 Health science degree Jobs in Missouri

cGMP Manufacturing Supervisor - Night Shift
MilliporeSigma —St. Louis, MO
- $88,800 - $152,300 a year
- 12 hour shift
- Mid-level
- Supervising experience
- Bachelor's degree
- Health insurance
- Paid time off
2d
Oncology Account Manager/Sr OAM - Kansas City MO
Genmab —Kansas City, MO
- $160,000 - $240,000 a year
- Online Application
- Private practice
- Microsoft Outlook
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Research Assistant
Syndicus Inc —Creve Coeur, MO
- Up to $32.26 an hour
- Contract
- Mid-level
- Bachelor's degree
- Cleaning
Quick Apply
1d
Case Manager - PRTF
KVC Health Systems —St. Louis, MO
- Full-time
- Clean driving record
- Microsoft Excel
- Microsoft Outlook
Quick Apply
11d
Technical Writer (GMP)
Yoh, A Day & Zimmermann Company —St. Louis, MO
- $30 - $37 an hour
- Mid-level
- 3 years
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
PROJECT MANAGER
BJC HealthCare —Fenton, MO
- $69,326.40 - $112,860.80 a year
- Full-time
- Hybrid work
- Mid-level
- Bachelor's degree
- Team management
- Disability insurance
- Health insurance
6d
CRA 1, IQVIA Biotech
IQVIA —Kansas City, MO
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
EHR Application I Analyst
BJC HealthCare —St. Louis, MO
- $57,304 - $93,288 a year
- Full-time
- Remote
- High school diploma or GED
- Bachelor's degree
- Children
- Disability insurance
- Health insurance
5h
Medical Science Liaison
Alumis —Kansas City, MO
- Up to $235,000 a year
- Weekends as needed
- Remote
- Up to 50% travel
- Writing skills
- 3 years
- Health insurance
- Cell phone reimbursement
Quick Apply
Coordinator Field Research - Infectious Diseases
Washington University in St. Louis —St. Louis, MO
- $54,600 - $81,900 a year
- Online Application
- Pass drug screening
- Mid-level
- Office
- Commuter assistance
- Employee assistance program
Entry Level Environmental Remediation Professional -Central/Midwest United States- Hybrid
Jacobs —St. Louis, MO
- $58,656 - $88,000 a year
- Hybrid work
- Office
- Driver's License
- Bachelor's degree
- Paid holidays
- Health insurance
Health Information Technology Specialist Central
IQVIA —Kansas City, MO
- $125,000 - $135,000 a year
- Full-time
- System design
- Mid-level
- Master's degree
Contract Mgr. II - health plans
BJC HealthCare —St. Louis, MO
- $69,326.40 - $112,860.80 a year
- Full-time
- Mid-level
- Bachelor's degree
- Children
- Disability insurance
- Health insurance
Regulatory Coordinator - Cancer Center
The University of Kansas Medical Center —Kansas City, MO
- $28.20 - $38.35 an hour
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Paid jury duty
- Paid holidays
12d
Research Specialist I
Children's Mercy KC —Kansas City, MO
- From $26.62 an hour
- Full-time
- Pass drug screening
- Research
- Master's degree
Science & Medicine Advisor
American Heart Association —St. Louis, MO
- $110,000 - $120,000 a year
- Full-time
- Medicine
- Office
- Doctor of Philosophy
- Wellness program
- Paid holidays
Sponsorship & Events Strategist
BJC HealthCare —St. Louis, MO
- $63,024.00 - $102,627.20 a year
- Weekends as needed
- Hybrid work
- Hospital
- Mid-level
- Office
- Disability insurance
- Health insurance
Clinical Research Assistant II
Children's Mercy KC —Kansas City, MO
- From $24.14 an hour
- Full-time
- Pass drug screening
- Mid-level
- 3 years
Clinical Implementation Science Lead
SSM Health —St. Louis, MO
- Full-time
- 5 years
- Bachelor's degree
- Children
- Paid parental leave
- Health insurance
Customer Engagement Strategist
The Cigna Group —St. Louis, MO
- $108,400 - $180,600 a year
- Online Application
- 5 years
- Bachelor's degree
- Fair chance
- Paid holidays
- Health insurance

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cGMP Manufacturing Supervisor - Night Shift

MilliporeSigma -
St. Louis, MO

Apply Now

Job Details

$88,800 - $152,300 a year
2 days ago

Benefits

Health insurance
Paid time off

Qualifications

Team leadership
Manufacturing facility experience
Supervising experience
Bachelor's degree
Managing manufacturing teams
Pharmaceutical manufacturing facility experience

Full Job Description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

At MilliporeSigma, as the cGMP Manufacturing Supervisor – Night Shift at our 3300 South Second Ave / Cherokee site, will manage production personnel in the manufacture of products and many support functions outside of manufacturing. Job duties include:

12 hour night shift (7:00pm - 7:30am) shifts with a 20% shift differential
Oversee the manufacturing of Active Pharmaceutical Ingredients (API’s) regulated by the Food and Drug Administration and other regulatory bodies.
This position will have direct reporting structures for scientists engaged in supporting the manufacturing operations, production coordinator, and manufacturing training program.
Provide guidance Monday – Friday for scientists engaged in production readiness, including batch record review, equipment procurement, material transfer, training oversight and employee scheduling.
This position will be overseeing a manufacturing training team currently consisting of people on rotating shifts (Day and Night Shift).
This position will oversee a manufacturing coordination team consisting of people working Monday-Friday. Team responsibility includes material transfers from warehouse, material returns, and material consumptions.
This position will have the primary purpose of ensuring goods receipts are performed in a timely manner after manufacturing campaign is complete.
Lead a team of production scientists and operators in the scale-up, technology transfer, and execution of cGMP manufacturing.
Develop employees’ knowledge and skills to improve performance and expand abilities as well as to coordinate the group’s efforts to assist meeting the departmental, company, and customer’s objectives.
Adhere to protocols consistent with, and established according to, current Good Manufacturing Practices.
Collaboration is important. Work cross-functionally with Project Management, MSAT, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
Interact with our customers’ project management, technical and quality teams.
Maintain departmental goals and objectives in a safe manner and in compliance with all applicable federal, state, and company regulations (OSHA, EPA, FDA, EMA etc.).
Responsible for the management of capital for equipment and facility improvements, including balancing the departmental budget. A primary responsibility will be the creation of purchasing Process Orders.
Support department efforts toward Process Improvement and company goals.
Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
Ensure employees remain current with all department and site training requirements.
Assist and/or Lead root cause investigations and implement effective corrective and preventative actions related to manufacturing deviations.
Provide leadership and support of safety initiatives within production operations to ensure compliance with OSHA requirements.
Ensure tasks are done in accordance with approved site procedures, batch records and protocols.

Who You Are

Minimum Qualifications:

Bachelor’s Degree in Chemistry, Biology, Biochemistry, Chemical Engineering, or other Life Science disciplines.
4+ years of manufacturing experience in a cGMP setting.
1+ years of Management, Supervisory, or Lead experience.

Preferred Qualifications:

3+ years of Management, Supervisory, or Lead experience in GxP environment.
Customer interfacing audit experience.
Knowledge of Six Sigma concepts/Lean Manufacturing or process improvement.
Familiarity with large scale cGMP process equipment, tangential flow, and chromatography automation.
Strong Microsoft Office experience for Manufacturing/Operating procedure writing, technical report generation, product tracking and trending data analysis and Operational Excellence reports.
Strong interpersonal skills and conflict resolution experience
Advanced written and verbal communication skills.

RSREMD

Pay Range for this position: $88,800 - $152,300 a year.

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Apply Now

Refine Your Search

health science degree jobs in missouri

cGMP Manufacturing Supervisor - Night Shift

Oncology Account Manager/Sr OAM - Kansas City MO

Research Assistant

Case Manager - PRTF

Technical Writer (GMP)

PROJECT MANAGER

CRA 1, IQVIA Biotech

EHR Application I Analyst

Medical Science Liaison

Coordinator Field Research - Infectious Diseases

Entry Level Environmental Remediation Professional -Central/Midwest United States- Hybrid

Health Information Technology Specialist Central

Contract Mgr. II - health plans

Regulatory Coordinator - Cancer Center

Research Specialist I

Science & Medicine Advisor

Sponsorship & Events Strategist

Clinical Research Assistant II

Clinical Implementation Science Lead

Customer Engagement Strategist

I want to receive the latest job alert for health science degree in missouri

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