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Associate Process Development Scientist Jobs in Dublin, NH

Merck Group

Process Engineer 1

Jaffrey, NH · On-site

$72K - $110K/yr

Our colleagues across the globe love innovating with science and technology to enrich people ... development, review, and execution), and manages change requests by initiating, reviewing, and ...

New

Merck

Engineering Supervisor

Jaffrey, NH

... are, Life Science and Electronics. For more than 350 years and across the world we have ... Experience with automated fluid skids, web processes, and process development in a cGMP environment.

Merck Group

Senior Process Engineer

Jaffrey, NH · On-site

$100K - $130K/yr

... development and execution within the Life Science (LS) sector. This position will be based at our Jaffrey, New Hampshire site within ISCO Engineering & Technology (E&T), Global Process Engineering ...

Amphenol TCS

Process Engineer

Nashua, NH · On-site

ACS has an expansive global presence in research and development, manufacturing, and sales. We ... Bachelor's degree in Materials Science, Chemical Engineering, Chemistry, Mechanical Engineering, or ...

Peraton Labs

Principal Research Scientist

Bedford, NH · On-site

$176K - $282K/yr

Strong research background and development experience in cybersecurity, networking, communications ... process to verify your identity. EEO: Equal opportunity employer, including disability and ...

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All JobsAssociate Process Development Scientist JobsAssociate Process Development Scientist Jobs in Dublin, NH

Associate Process Development Scientist information

See Dublin, NH salary details

$18

$36

$58

How much do associate process development scientist jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for associate process development scientist in Dublin, NH is $36.34, according to ZipRecruiter salary data. Most workers in this role earn between $28.22 and $41.35 per hour, depending on experience, location, and employer.

What is the difference between Associate Process Development Scientist vs Process Development Scientist?

AspectAssociate Process Development ScientistProcess Development Scientist
Required CredentialsBachelor's or Master's in Life Sciences or Chemical EngineeringBachelor's or Master's, often with more experience or specialization
Work EnvironmentEntry-level, supporting process optimization in labs or manufacturingMore independent, leading process improvements and validations
Employer & Industry UsagePharmaceutical, biotech, or biotech manufacturing companiesSame industries, with increased responsibilities

The Associate Process Development Scientist typically supports process development tasks under supervision, focusing on experimental execution. In contrast, the Process Development Scientist takes on more independent roles, leading projects and process improvements. Both roles are common in biotech and pharmaceutical industries, with the main difference being experience level and scope of responsibilities.

Associate Process Development Scientist jobs near you
Infographic showing various Associate Process Development Scientist job openings in Dublin, NH as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $75,577 per year, or $36.3 per hour.
Scientist I - Process Development

Scientist I - Process Development

PCI Pharma Services

Bedford, NH • On-site

Full-time

Re-posted 18 days ago

PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

435th of 527 rated manufacturers

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
JOB SUMMARY -
The Scientist I position supports the efforts of the Process Development department within a fast-paced, expanding CDMO. This job will require extensive laboratory work, testing, and strategic client support of pharmaceutical development projects.
JOB DUTIES -
  • Support Process Development projects, serving as a SME and collaborator for formulation and process design activities.
  • Support senior scientists in performing experiments to achieve project milestones.
  • Act as a Process Development representative on internal and client-facing project calls, providing technical updates and strategic input.
  • Support the formulation design, sterile filtration, lyophilization, and post-processing for both small molecules and biologics, including antibody-drug conjugates (ADCs) and other complex modalities.
  • Support technology transfer activities and assist in scale-up or manufacturing transitions.
  • Executor of in-process and finished product testing within the Process Development laboratory, utilizing methods such as HPLC/UPLC, UV-Vis spectroscopy, Flowcam, Karl Fischer titration, DSC/FDM, and other related assays to confirm acceptance criteria.
  • Ensure proper maintenance, calibration, and cleanliness of laboratory instruments and equipment.
  • Perform or assist in routine facilities cleaning and equipment upkeep as required.
  • Draft and review Process Development batch records, protocols, and reports to ensure technical accuracy and compliance with internal quality standards.
  • Draft and maintain Standard Operating Procedures (SOPs) and related controlled documents for Process Development operations.
  • Collaborate cross-functionally with internal stakeholders including Quality Control (QC), Manufacturing Technical Services (MTS), and Operations, as well as external client teams, to ensure alignment and successful project execution.

PROFESSIONAL SKILLS -
  • Requires proficient laboratory and wet chemistry skills
  • Knowledge of current Good Manufacturing Processes (cGMP), Regulatory Guidelines, Aseptic Manufacturing, as well as bulk intermediate and medical device manufacturing.
  • Works independently with little direction; demonstrates a proven track record of leading tasks to completion.
  • Must consistently exhibit positive, effective interpersonal skills with internal and external teams, including relationship management of clients.
  • Ability to prioritize multiple ongoing projects and activities to meet customer and company timelines
  • Demonstrates excellent oral and written communication skills and can provide detailed project updates (PowerPoint) to clients and other internal departments efficiently and concisely.
  • Requires excellent organizational and interpersonal skills, team-player

EDUCATION/EXPERIENCE -
  • BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 0-5 years' experience in pharmaceutical development or CDMO industry
  • A desire to work in clinical-phase development and analytical characterization of drug products, including biologics
  • Experience with MS Office (Word/Excel/Teams/PowerPoint/SharePoint), SmartSheets, LabX, and Empower

QUALITIES -
  • Detail oriented and a results driven team player
  • Ability to work in a dynamic, fast paced work environment
  • Honesty, integrity, respect and courtesy with all colleagues
  • Creative with the ability to work with minimal supervision and balanced with independent thinking
  • Resilient through operational and organizational change

PHYSICAL REQUIREMENTS -
  • Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes.
  • Ability to gown and gain entry to controlled manufacturing areas.
  • Ability to lift, pull or push equipment requiring up to 25-50 lbs of force
  • Ability to stand for prolong periods in a production suite and work extended hours.

COMMUNICATIONS & CONTACTS -
  • Works directly with Process Development personnel
  • Works closely with QCAD, VAL, MTS, and Operations
  • Will interact with Customers on a regular basis
  • TRAVEL - < 10%

MANAGERIAL & SUPERVISORY RESPONSIBILITIES -
  • Required to lead and train junior level Process Development Scientists positions.

#LI-AK2
Join us and be part of building the bridge between life changing therapies and patients. Let's talk future
Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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