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Pharmaceutical Development Jobs in Michigan (NOW HIRING)

JobRx, Inc.

Director, Process Development

Riverview, MI · On-site

$150 - $190/hr

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 ...

MMS

Senior Statistical Programmer - Remote

Canton, MI · On-site

Hands-on experience with clinical trial and pharmaceutical development preferred. * Good communication skills and willingness to work with others to clearly understand needs and solve problems.

MMS

Senior Nonclinical Writer (US)

Canton, MI · On-site

Hands-on experience with clinical trial and pharmaceutical development preferred. * Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process. Powered ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

Hands-on experience with clinical trial and pharmaceutical development preferred * Basic understanding of CROs and scientific & nonclinical data/terminology, & the drug development process

Piramal Pharma Limited

Chemical Operator

Riverview, MI · On-site

$17.25 - $19.50/hr

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 ...

Piramal Pharma Limited

Chemical Operator

Riverview, MI · On-site

$17.25 - $19.50/hr

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 ...

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Pharmaceutical Development information

See Michigan salary details

$20.5K

$59.6K

$114.2K

How much do pharmaceutical development jobs pay per year?

As of Aug 27, 2026, the average yearly pay for pharmaceutical development in Michigan is $59,634.00, according to ZipRecruiter salary data. Most workers in this role earn between $30,500.00 and $77,600.00 per year, depending on experience, location, and employer.

What is a pharmaceutical development?

A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.

What does a pharmaceutical development professional do?

Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.

What are the key skills and qualifications needed to thrive in pharmaceutical development?

To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.

How much do pharmaceutical developers make?

Pharmaceutical developers typically earn a median annual salary of around $80,000 to $120,000, depending on experience, education, and location. Entry-level positions may start lower, while experienced professionals or those with advanced degrees can earn higher salaries, especially in research and development environments.

How to get into pharmaceutical development?

To enter pharmaceutical development, candidates typically need a bachelor's degree in pharmacy, chemistry, biology, or a related field, with advanced roles often requiring a master's or Ph.D. in a relevant discipline. Gaining experience through internships, research projects, or entry-level positions in laboratories is valuable, along with developing skills in laboratory techniques, data analysis, and regulatory compliance. Certifications such as Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP) can enhance job prospects in this field.

What does a pharmaceutical development do?

A pharmaceutical development professional is responsible for designing, testing, and optimizing processes to create new drugs or improve existing ones. They work in laboratories and manufacturing settings, often using specialized tools and adhering to regulatory standards to ensure product safety and efficacy.

What are the most commonly searched types of Pharmaceutical Development jobs in Michigan?

The most popular types of Pharmaceutical Development jobs in Michigan are:

What are popular job titles related to Pharmaceutical Development jobs in Michigan?

For Pharmaceutical Development jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Development jobs in Michigan look for?

The top searched job categories for Pharmaceutical Development jobs in Michigan are:

What cities in Michigan are hiring for Pharmaceutical Development jobs?

Cities in Michigan with the most Pharmaceutical Development job openings:

Pharmaceutical Development jobs near you
Infographic showing various Pharmaceutical Development job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $59,634 per year, or $28.7 per hour.

Process Development Scientist

Piramal Pharma Limited

Riverview, MI • On-site

Full-time

Re-posted 11 days ago

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

Process Development Scientist

Job Description

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility, located in Riverview, Michigan, is seeking a qualified Process Development Scientist to join our Process Development team. The PD Scientist is responsible for the development of current and new manufacturing processes.

Key responsibilities.

  • Develop, conduct, and/or manage the process development of current and new synthetic/process pathways including routine analytical testing to monitor process progress (HPLC, NMR, XRPD, GC-HS, KF, etc.).
  • Handling of highly potent compounds and experience in synthesis and handling of Linker-Payloads is highly desirable.
  • Scale-up preparative HPLC purification and lyophilization of intermediates and final products.
  • Maintain communications with clients and ensure their requirements are met.
  • Manage/support the production of new (HP)APIs. Ensure that adequate supplies of process materials (raw materials, solvents, reagents, etc.) and operation equipment (hoses, reactors, glassware, etc.) are available for assigned tasks.
  • Ensure that product shipments meet customer and regulatory (FDA, EPA, OSHA, etc.) requirements.
  • Write progress reports and provide technical support in meetings regarding current API production and new API process development.
  • Ensure that approved processes are carried out according to cGMP guidelines and are properly documented.
  • Keep Quality Assurance and Quality Control departments updated in regard to project/client requirements and schedules. Participate in the development, training, and transfer of new processes into the plant. Maintain accurate inventories of materials.
  • Prepare appropriate reports as needed for management and/or clients.
  • Maintain notebooks for research and development and non-GMP activities. Complete and audit production and cleaning records. Complete logbooks and documentation (dispensing record, BPRs, cleaning records, deviation reports, etc.) related to production and cleaning is accordance with regulatory requirements.
  • Generate and/or evaluate standard operating procedures as required.
  • Provide technical support for chemical operators, engineering, quality control, etc.

EDUCATION/EXPERIENCE

  • To be qualified as a PD Scientist, a candidate must have:
    • PhD in Organic or Medicinal Chemistry and up to four (4) years' experience in a relevant field; OR
    • MS in Organic or Medicinal Chemistry and up to eight (8) years' experience in a relevant field; OR
    • BS in Organic or Medicinal Chemistry and up to twelve (12) years' experience in a relevant field
  • Knowledge of organic chemistry and chemical safety.

job competencies.

  • Excellent organizational and planning skills.
  • Strong written, verbal, and interpersonal communication skills.
  • Self-motivated, creative, and independent.
  • Ability to direct projects covering a variety of chemical compounds including high potent APIs.
  • Familiarity with cGMP, plant safety, and EPA requirements.

Apply