This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
This position works closely with Project Managers, Filling and Finishing Operations, Quality ... Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech ...
... in the biotechnology, pharmaceutical or health related industry, including some project and people management experience. * Advanced SAS programming skills in a clinical data environment with ...
... in the biotechnology, pharmaceutical or health related industry, including some project and people management experience. * Advanced SAS programming skills in a clinical data environment with ...
Senior Director - Operations
Muskegon, MI · On-site
You would be joininga multi-billion-dollar global leader in biotechnology as the SeniorDirector ... Oversee Operational Execution Across Project Workstreams Manage the daily operations of multiple ...
Senior Director - Operations
Muskegon, MI · On-site
You would be joininga multi-billion-dollar global leader in biotechnology as the SeniorDirector ... Oversee Operational Execution Across Project Workstreams Manage the daily operations of multiple ...
Patient Services Technical Manager
Detroit, MI · On-site
$114K - $115K/yr
Leveraging your expertise in patient services, you will interface between pharmaceutical, biotech ... You will design, implement and optimize patient support programs, define project roadmaps and ...
Patient Services Technical Manager
Detroit, MI · On-site
$114K - $115K/yr
Leveraging your expertise in patient services, you will interface between pharmaceutical, biotech ... You will design, implement and optimize patient support programs, define project roadmaps and ...
Principal Scientist, Biology
Ann Arbor, MI · On-site
... managing project teams to achieve goals. Responsibilities * Independently design and execute ... PhD in cell biology, molecular biology, immunology or a related field with 9+ years of biotech or ...
Principal Scientist, Biology
Ann Arbor, MI · On-site
... managing project teams to achieve goals. Responsibilities * Independently design and execute ... PhD in cell biology, molecular biology, immunology or a related field with 9+ years of biotech or ...
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Quick apply
Manager of Sterility Assurance
Brighton, MI · On-site
$107K - $129K/yr
... projects in a fast-paced work environment, 4. Excellent interpersonal skills with the ability to ... the biotech / pharmaceutical industry, with 2+ years in Sterility Assurance / Environmental ...
Senior Quality Systems Specialist
Lansing, MI · On-site
$75K - $103K/yr
... biotech environments * Demonstrated experience with the following: * Managing complex quality ... Possesses strong organizational and project management skills for self and teams * Possesses a ...
Senior Quality Systems Specialist
Lansing, MI · On-site
$75K - $103K/yr
... biotech environments * Demonstrated experience with the following: * Managing complex quality ... Possesses strong organizational and project management skills for self and teams * Possesses a ...
Our solutions are used by customers across pharmaceutical, biotechnology, academic, government ... Excellent project management and organizational capabilities * Strong leadership and team ...
Our solutions are used by customers across pharmaceutical, biotechnology, academic, government ... Excellent project management and organizational capabilities * Strong leadership and team ...
You will be expected to lead project workstreams, manage and advise client stakeholders, lead teams ... biotech, and/or medical devices, including regulated supply chain environments and product ...
You will be expected to lead project workstreams, manage and advise client stakeholders, lead teams ... biotech, and/or medical devices, including regulated supply chain environments and product ...
Accounting Manager
Grand Rapids, MI · On-site
Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred
Accounting Manager
Grand Rapids, MI · On-site
Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred
You will be expected to lead project workstreams, manage and advise client stakeholders, lead teams ... biotech, and/or medical devices, including regulated supply chain environments and product ...
You will be expected to lead project workstreams, manage and advise client stakeholders, lead teams ... biotech, and/or medical devices, including regulated supply chain environments and product ...
Sr. Compliance Specialist
Grand Rapids, MI · On-site
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
Sr. Compliance Specialist
Grand Rapids, MI · On-site
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred
Lead accounting for capital projects, including grants, incentives, fixed assets, depreciation, and ... Experience in biotech, pharmaceutical, healthcare, or other regulated environments preferred
Sr. Compliance Specialist
Grand Rapids, MI · On-site
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
Sr. Compliance Specialist
Grand Rapids, MI · On-site
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
... biopharma and/or biotech. manufacturing environment. * Knowledge of current Food and Drug ... Prior project management experience is preferred. * Prior experience with aseptic processes and ...
Head of Validation
Brighton, MI · On-site
... biotechnology, or regulated manufacturing environments * Prior leadership experience within ... management, and 21 CFR Part 11 requirements * Hands-on experience leading validation projects and ...
Quick apply
Head of Validation
Brighton, MI · On-site
... biotechnology, or regulated manufacturing environments * Prior leadership experience within ... management, and 21 CFR Part 11 requirements * Hands-on experience leading validation projects and ...
Project Manager Biotech information
See Michigan salary details
$19.07 - $23.39
4% of jobs
$23.39 - $27.71
8% of jobs
$27.71 - $32.04
3% of jobs
$33.93 is the 25th percentile. Wages below this are outliers.
$32.04 - $36.36
21% of jobs
The median wage is $39.06 / hr.
$36.36 - $40.68
21% of jobs
$43.61 is the 75th percentile. Wages above this are outliers.
$40.68 - $45.01
25% of jobs
$45.01 - $49.33
13% of jobs
$49.33 - $53.66
2% of jobs
$53.66 - $57.98
1% of jobs
$57.98 - $62.30
1% of jobs
$62.30 - $66.63
0% of jobs
$19
$40
$66
How much do project manager biotech jobs pay per hour?
What is the difference between Project Manager Biotech vs Clinical Project Manager?
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.
How does a Project Manager in biotech typically collaborate with cross-functional teams to drive project success?
What does a Project Manager in Biotech do?
What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?
Other
Medical, Dental, Vision, Life, Retirement, PTO
Posted 21 days ago
Job description
Description
Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!
Overview of this Position:
Provides quality support to both internal and external projects, including the on-boarding of new clients / client projects, capital expenditures (CAPEX), continuous improvement initiatives, and as required in routine manufacturing and finishing operations. This position works closely with Project Managers, Filling and Finishing Operations, Quality Assurance Operations, Analytical Technical Services, Manufacturing Science & Technology, Validation, and QC Analytical and Microbiology departments. This is not a remote role.Â
Non-Negotiable Requirements:
- Completion of a bachelor's degree in Life Sciences or a related field and/or a minimum of 1-3 years of related work experience for a Specialist I, 3-5 years for a Specialist II, 5-7 for a Specialist III, and 7+ years for a Sr. Specialist.Â
- Experience and expertise of QA principles and procedures in pharma, biopharma, and/or biotech manufacturing environment or manufacturing environment of regulated products with a thorough understanding of cGMP, FDA guidelines and multinational regulatory standards.Â
- Proficient computer skills in Microsoft Word, Excel, and Outlook.Â
Preferred Requirements:
- QA Experience and expertise in aseptic environment.
Responsibilities Include (but are not limited to):
- Provide working knowledge of GMP and regulatory requirements as it relates to performing Quality Assurance review and approval of cGMP documentation in support of GRAM and client-driven projects including:Â
- Standard Operating Procedures
- Test Methods
- Raw Material, Component, and Finished Product Specifications
- Risk Assessments including change control assessments
- Master Batch Records
- Validation Documents
- Provide review of executed batch records in relation to initial technical transfer and process performance qualifications.Â
- Support current clients and on-boarding of new client projects.Â
- Manage Quality deliverables according to project schedules and ensure tasks assigned are delivered according to project timeline.
- Ensure that project deliverables meet all regulatory and industry best practice standards.
- QA representative on project teams to ensure that project deliverables meet all regulatory and industry best practice standards as well as internal deadlines.Â
- Participate in deviation investigation teams to support quality investigations (NCR, LIR, SQIR, etc.).Â
Full job description available during formal interview process.
What Sets GRAM Apart from Other Employers:
BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PTO: Full-time employees accrue up to 13 days of time off per calendar year. You choose how to use this time for your vacation, sick, or mental health needs!
WELLNESS TIME OFF: Employees earn 1 hour of time off for every 30 hours worked to use how you choose.Â
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
PAY: Depends on Experience and is discussed during the interview process.
If you meet the required criteria listed above, GRAM welcomes you to apply today!About GRAND RIVER ASEPTIC MANUFACTURING
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
51 - 200 Employees
Headquarters location
Grand Rapids, MI, US
Year founded
2011