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Pharmaceutical Process Development Jobs in Pennsylvania

GSK

Small Molecule Drug Substance Lead

King Of Prussia, PA · On-site

$149K - $248K/yr

Bachelor's degree in chemistry, chemical engineering, pharmaceutical sciences, or related field. * Minimum 10 years industry experience in small molecule drug substance process development, scale-up ...

USWM, LLC

Associate Scientist - MSAT

Philadelphia, PA · On-site

$70K - $110K/yr

... of process development and clinical/commercial production. The associate scientist will be ... pharmaceutical industry, Core competencies: * Experience working with closed-system, manual, and ...

DPS Group

Process SME

Conshohocken, PA · On-site

... Pharmaceutical and Biotechnology industry, specifically, Antibody Drug Conjugate (ADC ... Maintains current knowledge of relevant developments in their professional area of expertise

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Pharmaceutical Process Development information

What is the difference between Pharmaceutical Process Development vs Pharmaceutical Manufacturing Technician?

AspectPharmaceutical Process DevelopmentPharmaceutical Manufacturing Technician
Primary FocusDesigning, optimizing, and scaling up manufacturing processes for new or existing drugsOperating equipment, assembling products, and ensuring production runs smoothly
Work EnvironmentLaboratories, R&D facilities, pilot plantsProduction floors, manufacturing plants
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; experience in process developmentHigh school diploma or equivalent; on-the-job training

Pharmaceutical Process Development focuses on creating and refining manufacturing processes, while Pharmaceutical Manufacturing Technicians handle the day-to-day production tasks. Both roles are essential in the drug development and manufacturing pipeline, but they differ in scope, responsibilities, and work environment.

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

To thrive in Pharmaceutical Process Development, you need a solid background in chemical engineering, pharmaceutical sciences, or a related field, often supported by an advanced degree. Familiarity with process analytical technology (PAT), Good Manufacturing Practice (GMP) standards, and software like MATLAB or SIMCA is typically required. Strong problem-solving, teamwork, and communication skills help professionals navigate complex projects and cross-functional collaborations. These skills are crucial for ensuring efficient, compliant, and innovative drug development processes that meet regulatory requirements and industry standards.

What are the typical challenges faced when transitioning a pharmaceutical process from laboratory scale to full-scale manufacturing?

One of the main challenges in pharmaceutical process development is ensuring that processes developed at laboratory or pilot scale remain robust, efficient, and compliant when scaled up to full manufacturing. Variables such as mixing, temperature control, and material properties can behave differently at larger volumes, potentially impacting product quality or yield. Process developers often work closely with manufacturing, quality assurance, and engineering teams to troubleshoot issues and optimize protocols, making strong cross-functional collaboration skills essential. Addressing regulatory requirements during scale-up is also critical to ensure that the process meets all quality and safety standards.

What is pharmaceutical process development?

Pharmaceutical process development is the series of activities involved in designing, optimizing, and scaling up the manufacturing processes for pharmaceutical products. It includes transforming laboratory procedures into reliable, efficient, and reproducible processes that meet regulatory standards for quality and safety. This phase is crucial for ensuring that medications can be produced consistently and at a larger scale while maintaining product efficacy and compliance with industry regulations.

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

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

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

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

Pharmaceutical Process Development jobs near you
Infographic showing various Pharmaceutical Process Development job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Senior Specialist, Regulatory Affairs, Medical Devices

West Pharmaceutical Services

Exton, PA • On-site

Full-time

Posted 22 days ago

West Pharmaceutical Services rating

8.5

Company rating: 8.5 out of 10

Based on 32 frontline employees who took The Breakroom Quiz

12th of 119 rated packaging manufacturers

Job description

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week
Who We Are:
At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Job Summary
  • The Regulatory Affairs Sr. Specialist is responsible for influencing department regulatory processes and procedures, developing strategies, authoring, reviewing, and supporting global registrations, including Premarket Notifications, Post Market Submissions, China NMPA Registrations, Technical Documentation for CE Marking, technical packages.
  • The Sr. Specialist ensures timely and high-quality execution of all regulatory deliverables. In addition, the Sr. Specialist mentors team members and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements.
  • This position includes supporting internal and external customer regulatory requests.

Essential Duties and Responsibilities
  • Develop and implement medical device regulatory strategies for West's Transfer Devices with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in an efficient, compliant manner
  • Author and review US, EU, South Korea, China and additional international submissions with guidance for new products, product changes and post-market updates as required to ensure timely approvals for market release and file maintenance
  • Works with global Regulatory Affairs colleagues, Quality Assurance and Research & Development teams to ensure submissions are accurately prepared and comply with global regulations
  • Provide leadership to product development teams for regulatory issues and questions
  • Provide support to market-released products as necessary, including reviewing labeling, promotional material, product/manufacturing process changes, post-market reporting and documentation
  • Establish and maintain good working relationships with agency personnel
  • Compile and maintain regulatory databases or systems as well as technical documentation required for new or modified products
  • Write or update standard operating procedures, work instructions, or policies
  • Cleary and effectively communicate team/project progress/status, decisions, timelines, etc. to RA management, internal and external customers
  • Develop specific objectives and manage work assignments, with minimal guidance to achieve personal objectives in conformance with overall business goals
  • Maintain effectiveness when experiencing major changes in work responsibilities or environment adjusting effectively to work within new work structures, processes, requirements, or cultures
  • Challenge processes, remain open to ideas and changes to continuously improve, seek better alternatives, and drive change
  • Adhere to all applicable government and West regulations, practices, and procedures to maintain compliance
  • Other duties as assigned

Education
  • Education: Bachelor's, Master's degree or PhD in science, math, engineering, or related discipline or equivalent experience

Work Experience
  • Bachelor's with 5+ years; Master's degree/PhD with 3+ years of medical device, pharmaceutical or regulatory experience

Preferred Knowledge, Skills and Abilities
  • Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
  • Able to comply with the company's safety and quality policy at all times
  • International regulatory competency
  • Attention to detail with planning, time management and organizational skills
  • Knowledge of 21 CFR 820/ISO 13485
  • Possesses technical leadership skills, as well as demonstrated understanding of related medical device and pharmaceutical operations (e.g., manufacturing, process development, analytical, quality assurance).
  • Maintain working knowledge of computer software packages including MS Word, MS Excel, MS PowerPoint, Master Control, Adobe, SharePoint, MS Teams, Outlook, and others as required
  • Experience directly interacting and presenting to project teams and customers
  • Strong negotiation and decision-making skills
  • Excellent written and verbal communication, timeline management skill
  • Self-motivated with a proactive attitude and the ability to work effectively
  • Regulatory compliance competency including Quality Systems
  • R.A.C certification(s)

License and Certifications
  • Regulatory Affairs Certifications (RAC)-RAPS R.A.C certification(s) preferred

Travel Requirements
10%: Up to 26 business days per year
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Ability to comprehend principles of math, science, engineering, and medical device use.
  • Ability to handle technical reports, drawings, specifications, regulatory and quality documentation with a high degree of confidentiality.
  • Ability to research, read, analyze, and interpret regulatory literature and documentation, regulations, technical standards, guidance documents, test reports, clinical/medical terminology, technical product information, and complex documents.
  • Ability to review, collate, describe, and summarize scientific and technical data.
  • Ability to organize complex information and combine pieces of information to form general rules or conclusions.
  • Ability to utilize judgment and make decisions considering the relative risks and benefits of potential actions to choose the most appropriate one.
  • Ability to assess, plan, schedule and manage multiple long-term and short-term projects, tasks, responsibilities and/or priorities in a concurrent fashion with several parallel deliverables and execute deliverables to time-line commitments.
  • Ability to be an effective team member and work well with others in a team environment on cross- functional and/or matrix teams.

#LI-DJ1 #LI-HYBRID
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

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