You're Viewing 1 Of 95,000+ Jobs On OysterLink
New hospitality jobs added daily. Browse by role, pay, or location.
Job Overview
Employment Type
Full-time
Compensation
Hourly
Range $26.00 - $45.00
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Paid Time Off
Retirement Plan
Professional Development
Employee assistance program
performance bonuses
Job Description
Piramal Pharma Solutions is a leading contract development and manufacturing organization (CDMO) specializing in providing end-to-end development and manufacturing solutions across the entire drug life cycle. With a comprehensive global network of facilities spanning North America, Europe, and Asia, Piramal Pharma Solutions supports innovator and generic pharmaceutical companies worldwide by delivering a wide range of services. These include drug discovery solutions, process and pharmaceutical development services, clinical trial supplies, and commercial supply of active pharmaceutical ingredients (APIs) and finished dosage forms. Additionally, the company offers specialized services such as the development and manufacture of highly potent APIs and antibody drug... Show More
Job Requirements
- BS degree in chemistry, biochemistry, pharmaceutical science or related field
- Minimum 2 years of industry experience in pharmaceutical formulation development
- Experience with sterile injectable dosage forms development
- Familiarity with lyophilization processes and suspension development
- Proficient in experimental design and statistical analysis
- Ability to work collaboratively in cross-functional teams
- Strong problem-solving and communication skills
- Experience in clinical or commercial manufacturing environments
- Knowledge of analytical methodologies such as HPLC, Karl Fischer titration, particulate matter analysis
- Comfort working in a dynamic matrix organizational structure
- Ability to manage multiple projects and timelines
- Adaptability to changing project priorities and environments
Job Qualifications
- BS in chemistry, biochemistry or pharmaceutical science or related discipline
- 2+ years industry experience focusing on developing parenteral, solid and/or other formulation applications
- Experience working within a variety of dosage forms including parenterals, lyophiles, polymers, suspensions, drug delivery systems
- Knowledge of design of experiments, statistics, and unique technologies
- Experience with lyophilization cycle development and suspension development
- Experience working within a clinical or commercial manufacturing organization
- Knowledge of relevant analytical techniques required for formulation and product analysis
- Ability to serve interdisciplinary and multidisciplinary teams
- Strong technical aptitude
- Excellent organizational, technical, and creative problem solving skills
- Proficiency in statistical evaluation of data and design of experiments
- Flexible and adaptable to changing priorities
- Comfortable working in a matrix environment
Job Duties
- Design studies related to pre-formulation and formulation of parenteral products including solubility, pH solution stability, lyophilization, suspension development, polymer development and others that impact stability and delivery of the product
- Experimental design, data evaluation, generation of scientific reports, and coordination of studies with other technical groups
- Play an important role in scale-up and technology transfer process in collaboration with Manufacturing team
- Investigate, troubleshoot and resolve issues associated with formulation studies and/or R&D pilot manufacturing
- Develop and track project timelines and assume departmental responsibilities for projects when necessary
- Consult and interact with internal cross-functional teams and external clients and customers
- Operate equipment and apply analytical methodology utilized in formulation development of parenteral dosage forms such as lyophilizers, compounding/filling equipment, mixing techniques, sterilization techniques, HPLC, KF, particulate matter analysis
- Provide feasibility assessment for scientific principles and concepts for potential clients, products and investigations
- Conduct literature searches to support formulation development and pilot manufacturing documentation
- Communicate and defend work orally and in writing at team meetings, in technical documents, and to external partners
- Assist, consult, and troubleshoot during process transfer scale-up and validation activities
- Interpret results and scientific information including proficiency in statistical evaluation of data and design of experiments
- Interact with cross functional departments including Business Development, Project Management, ARD, QC, Process Development, Quality, Operations and with external clients
Job Criteria
Experience
Mid Level (3-7 years)
Job Location
Don't Stop At One Job - There's More
Create a free profile
We'll match you with best jobs
Get job offers faster
Search For More Opportunities:
More Jobs Like This: