Top 95 Pharmaceutical manufacturing Jobs in Detroit, Mi

Manager, Process Development
PPL Pharma Solutions Riverview LLC —Riverview, MI
- Full-time
- Doctor of Philosophy
- Senior level
- Communication skills
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Process Development Manager
Piramal Pharma Solutions —Riverview, MI
- Full-time
- Doctor of Philosophy
- In-person
- Senior level
- Relocation assistance
- Health insurance
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12d
Process Excellence Engineer
Piramal Pharma Solutions —Riverview, MI
- $100,000 a year
- Full-time
- 3 years
- Analysis skills
- Bachelor's degree
- Health savings account
- Health insurance
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Quality Control Chemist
Piramal Pharma Solutions —Riverview, MI
- Full-time
- OSHA
- Mid-level
- Analysis skills
- Health savings account
- Relocation assistance
Quick Apply
Quality Control Chemist - PM Shift
Piramal Pharma Solutions —Riverview, MI
- Full-time
- OSHA
- Mid-level
- Analysis skills
- Health savings account
- Relocation assistance
Quick Apply
Pharmaceutical Lab Technician
Siemens Healthineers —Royal Oak, MI
- $42,030 - $57,794 a year
- Overtime
- Customer service
- Word processing
- Computer literacy
- Paid training
- Disability insurance
Entry Level Quality Assurance Quality Control
Pure Herbs Ltd. —Sterling Heights, MI
- $18 - $25 an hour
- Full-time
- Bachelor's degree
- In-person
- Entry level
- Paid training
- Health insurance
Quick Apply
1d
Specialty Sales Rep - Primary Care
Alora Pharmaceuticals —Detroit, MI
- $65,000 - $80,000 a year
- Bachelor of Science
- Primary Care
- Mid-level
- Disability insurance
- Health insurance
Specialty Sales Rep - Primary Care
Acellapharma —Detroit, MI
- $65,000 - $80,000 a year
- Bachelor of Science
- Primary Care
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Nurse Consultant- Michigan
Bristol-Myers Squibb —Detroit, MI
- $142,710 - $172,927 a year
- Weekends as needed
- Hybrid work
- Nursing
- RN License
- 5 years
- Paid holidays
- Disability insurance
Territory Sales Manager - Detroit
Dechra Pharmaceuticals PLC —Detroit, MI
- $90,000 - $156,000 a year
- Up to 50% travel
- Mid-level
- Driver's License
- 401(k) matching
QA Inspector (pharmaceuticals and cosmetics)
Elba Laboratories —Troy, MI
- From $20 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Basic math
- Health insurance
- Dental insurance
Quick Apply
Process Development Scientist
PPL Pharma Solutions Riverview LLC —Riverview, MI
- Full-time
- Customer service
- Bachelor of Science
- Mid-level
Medical Science Liaison Immunology - Admilparant (Michigan)
Bristol-Myers Squibb —Detroit, MI
- $166,090 - $201,262 a year
- Email
- Hybrid work
- Medicine
- English
- Mid-level
- Paid holidays
- Disability insurance
Chemical Operator
PPL Pharma Solutions Riverview LLC —Riverview, MI
- High school diploma or GED
- Communication skills
- Mechanical knowledge
Compounding Specialist - Full Time
Merit Manufacturing —Warren, MI
- From $23 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Ability to lift 50 pounds
- Health insurance
- Dental insurance
Quick Apply
Quality Associate Specialist, Defect Characterization
Par Health —Rochester, MI
- Full-time
- Mid-level
- Continuous improvement
- Mentoring
4d
Medical Science Liaison, Cardiovascular - Milvexian (Michigan)
Bristol-Myers Squibb —Detroit, MI
- $166,090 - $201,262 a year
- Email
- Hybrid work
- Medicine
- English
- Mid-level
- Paid holidays
- Disability insurance
Business Development Associate - Biotec Solutions - San Francisco, CA & Midwest US
Thermo Fisher Scientific —Detroit, MI
- $82,500 - $123,750 a year
- Full-time
- Up to 50% travel
- 5 years
- Research
- Commuter assistance
- Paid parental leave
Senior Validation Engineer
Pfizer —Rochester, MI
- $82,700 - $137,900 a year
- Weekends as needed
- Bachelor of Science
- High school diploma or GED
- Analysis skills
- Paid holidays
- Relocation assistance
5d

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pharmaceutical manufacturing jobs near detroit, mi

Manager, Process Development

PPL Pharma Solutions Riverview LLC -
Riverview, MI

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Job Details

Full-time

Qualifications

Team leadership
Team development
Doctor of Philosophy
Project management software
Managing projects
Pharmaceutical research experience
Team building

Full Job Description

Be the First to Apply

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Manager, Process Development

Job Description

The Manager, Process Development will serve as a member of the technical leadership for the development of new processes for the synthesis of API or API candidates at both the Detroit and Riverview manufacturing facilities for Ash Stevens, LLC, a division of Piramal Pharma Solutions. The incumbent will help with the planning and organization of all activities in the Chemical Process Development department to ensure that timelines, specifications, cGMP requirements, and the other terms of contracts are fully respected. This position will also provide technical expertise at the request of the Head of Process Development and other departments and employees. You will collaborate and interact with the other departments of Ash Stevens (Quality Assurance, Quality Control, Safety, Engineering, Operations, etc.) so that all resources required for developing and approving a process are in place. Periodically this role will inform the client with the status of the project. This role will actively participate in potential new project assessments to provide Site Leadership with technical input regarding the feasibility of the project, and will also prepare technical reports and participate in the site management meetings/team.

Key accountabilities:

Assess new projects with the department in order to identify the best chemical route and resources to be used in order to develop a process.
Organize work within the department to ensure that timeliness, specifications, and FDA requirements are respected and correlate with most effective and economic use of the resources.
Conduct literature searches and laboratory work to quickly identify the potential and limitations of different routes and propose the optimal solution for development.
Contribute to the efforts to identify, characterize, and synthesize by-products and impurities generated in different steps of a process and find the conditions to diminish/suppress or remove them.
Direct the development of “in-process methods” to monitor chemical processes.
Provide technical opinions and recommendations to the members of the Process Development Department in order to elaborate chemical manufacturing processes that are safe, economical, and in compliance with cGMP requirements.
Work in the laboratory or plant (hands-on) as required.
Generate, verify, approve, and revise BPRs, specifications, deviation reports, and development reports.
Actively participate in technical talks to find solutions to different problems and carefully consider opinions and suggestions for future work.
Periodically interact with QA, QC, Engineering, Safety, and Operations departments to ensure all aspects of a project under development are being taken into consideration.
Identify and protect the original technical information as part of the company property.
Promote a friendly and cooperative environment for all members of the department in order to facilitate open communication. Strongly encourage teamwork and carefully consider and analyze other people’s opinions. Participate in meetings with potential clients and brokers to provide input to ASI’s Senior Management about technical aspects of potential business opportunities for the company. Interact with clients in a positive and constructive manner.
Work with clients for an efficient transfer and implementation of the technological /analytical information.
Actively participate in technical talks to find solutions to different problems and carefully consider other opinions and suggestions for future work.

EDUCATION/EXPERIENCE:

Ph.D. in Organic Chemistry, Medicinal Chemistry, or Chemical Engineering.
Minimum ten (10) years’ experience in research and chemical development of drugs and fine chemicals, with a proven track record of contribution in the field.
Wide knowledge of classic and modern synthetic methods (excluding Chemical Engineers).
Up to five (5) of successful track record of building and managing research teams.
Familiar with project management tools and best practices.

job competencies:

Able to direct and interact with team members.
Excellent organizational and planning skills.
Strong written, verbal, and interpersonal communication skills.
Have the ability to develop, perform, evaluate, and troubleshoot within a scientific discipline.
Self-motivated, creative, and independent.
Ability to manage projects covering a variety of chemical compounds.

Work Location: In person

Quick Apply

Refine Your Search

pharmaceutical manufacturing jobs in detroit, mi

Manager, Process Development

Process Development Manager

Process Excellence Engineer

Quality Control Chemist

Quality Control Chemist - PM Shift

Pharmaceutical Lab Technician

Entry Level Quality Assurance Quality Control

Specialty Sales Rep - Primary Care

Specialty Sales Rep - Primary Care

Clinical Nurse Consultant- Michigan

Territory Sales Manager - Detroit

QA Inspector (pharmaceuticals and cosmetics)

Process Development Scientist

Medical Science Liaison Immunology - Admilparant (Michigan)

Chemical Operator

Compounding Specialist - Full Time

Quality Associate Specialist, Defect Characterization

Medical Science Liaison, Cardiovascular - Milvexian (Michigan)

Business Development Associate - Biotec Solutions - San Francisco, CA & Midwest US

Senior Validation Engineer

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