location_onMumbai, Maharashtra, India
watch_later Posted: Apr 18, 2025
Job Description
Job Description
Business: Pharma Solutions
Department: Process Development
Location: Riverview, Michigan USA
Travel: NA
Job Overview
The Associate Process Development (PD) Scientist is responsible for the development of current and new manufacturing processes under the supervision of a senior member of the group.
Key Stakeholders: Internal : SLT
Key Stakeholders: External: Clients and Customers
Reporting Structure: Will report to Sr. Director, Chemical Process Development.Will have 0 reportees
Experience
To be qualified as a PD Associate, a candidate must have a Ph.D. in Chemistry, or Organic Chemistry and 0-3 years’ research experience or postdoctoral experience.
Excellent knowledge of organic chemistry and chemical safety.
Awareness of emerging Digital trends and their application within Quality context.
Required Skills And Competencies
Excellent organizational and planning skills.
Strong written, verbal, and interpersonal communication skills.
Self-motivated, creative, and independent.
Ability to work on projects covering a variety of chemical compounds with minimum supervision.
Familiarity with cGMP, plant safety, and EPA requirements is desired.
Responsibilities
Carries assigned tasks under the supervision of a senior member of the group.
Develop, conduct, and/or manage the process development of current and new synthetic/process pathways under minimal supervision.
Maintain communications with clients and ensure their requirements are met.
Manage the production of new 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.
Qualifications
To be qualified as a PD Associate, a candidate must have a Ph.D. in Chemistry, or Organic Chemistry and 0-3 years’ research experience or postdoctoral experience.
Job Info
Business: Pharma Solutions
Department: Process Development
Location: Riverview, Michigan USA
Travel: NA
Job Overview
The Associate Process Development (PD) Scientist is responsible for the development of current and new manufacturing processes under the supervision of a senior member of the group.
Key Stakeholders: Internal : SLT
Key Stakeholders: External: Clients and Customers
Reporting Structure: Will report to Sr. Director, Chemical Process Development.Will have 0 reportees
Experience
To be qualified as a PD Associate, a candidate must have a Ph.D. in Chemistry, or Organic Chemistry and 0-3 years’ research experience or postdoctoral experience.
Excellent knowledge of organic chemistry and chemical safety.
Awareness of emerging Digital trends and their application within Quality context.
Required Skills And Competencies
Excellent organizational and planning skills.
Strong written, verbal, and interpersonal communication skills.
Self-motivated, creative, and independent.
Ability to work on projects covering a variety of chemical compounds with minimum supervision.
Familiarity with cGMP, plant safety, and EPA requirements is desired.
Responsibilities
Carries assigned tasks under the supervision of a senior member of the group.
Develop, conduct, and/or manage the process development of current and new synthetic/process pathways under minimal supervision.
Maintain communications with clients and ensure their requirements are met.
Manage the production of new 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.
Qualifications
To be qualified as a PD Associate, a candidate must have a Ph.D. in Chemistry, or Organic Chemistry and 0-3 years’ research experience or postdoctoral experience.
Job Info
- Job Identification 8345
- Job Category R & D
- Posting Date 04/14/2025, 08:14 PM
- Degree Level Post PHD or Higher
- Job Schedule Full time
- Locations Ash Stevens LLC, Riverview, MI, 48193, US
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