About this opportunity
PCI Pharma Services lists this Scientist II - Process Development opportunity in bedford, New Hampshire. Review the employer’s description below for duties, qualifications and application requirements.
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 DUTIES
Lead Process Development projects, serving as the technical lead and SME for formulation and process design activities.
Supports more complex Process Development projects as a collaborator, working with a senior scientist to achieve project milestones
Execute and analyze experiments to achieve project milestones with minimal supervision.
Develop and implement phase-appropriate process development strategies aligned with program objectives and regulatory expectations.
Act as a Process Development representative on internal and client-facing project calls, providing technical updates and strategic input.
Demonstrate proficiency in formulation design, sterile filtration, lyophilization, and post-processing for both small molecules and biologics.
Develop and optimize processes for high-potency compounds, including antibody-drug conjugates (ADCs) and other complex modalities.
Support technology transfer activities and assist in scale-up or manufacturing transitions.
Perform in-process and finished product testing within the Process Development laboratory, such as HPLC/UPLC, UV-Vis spectroscopy, Flowcam, Karl Fischer titration, DSC/FDM, and other related assays to confirm acceptance criteria.
Troubleshoot analytical or process challenges and propose scientifically sound corrective actions.
Responsible for proper maintenance, calibration, and cleanliness of laboratory instruments and equipment.
Perform or assist in routine facilities cleaning and equipment upkeep as required.
Author and review Process Development batch records, protocols, and reports to ensure technical accuracy and compliance with quality standards and client demand.
Review executed documentation for accuracy and completeness prior to submission to management.
Draft and maintain Standard Operating Procedures (SOPs) and related controlled documents for Process Development operations.
Provide training, technical guidance, and mentorship to junior scientists and laboratory staff.
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 exemplary 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. Experience with lyophilization cycle design preferred.
Works independently with little direction; demonstrates a proven track record of leading tasks to completion.
Ability to learn new technologies and concepts and drive implementation in the laboratory
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
Advanced Degree in (PhD) in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 0-3 years' experience in pharmaceutical development or CDMO industry.
BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 5+ years' experience in pharmaceutical development or CDMO industry
A strong foundation in clinical-phase development and analytical characterization of drug products, including biologics and other complex modalities
In depth knowledge of biopharmaceutical and/or medical product regulation, formulation, filtration, filling, and lyophilization operations
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
MANAGERIAL & SUPERVISORY RESPONSIBILITIES
Required to lead and train junior level Process Development Scientists positions.
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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, res...
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Worksite address
bedford, NH, 03110, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.