Cambrex · 1 day ago
Associate Scientist (ARD)
Durham, NC
Full-time
Onsite
Senior Level
6+ years expCambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services. The Associate Scientist role involves executing analytical methods, providing analytical support, and developing methodologies while maintaining compliance with cGMP guidelines.
AnalyticsBiotechnologyInnovation ManagementManufacturingMarket ResearchPharmaceutical
Responsibilities
Execute analytical methods for in-process control, release testing and stability monitoring of bulk drug substances and drug products under cGMP guidelines
Independently develop and evaluate methodologies, design and implement experiments
Participates in experimental design, including development of methods and testing requirements to demonstrate method suitability
Maintains compliant records with little or no supervision
Able to write technical documents with assistance
Strong understanding and proficiency in use and maintenance of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks
Routinely participates in compliance meetings to ensure that client requests are within boundaries of compliance
Proficient with a broad range of laboratory techniques and actively investigate new technologies
Attend and may participate in national and international scientific meetings
Independently plan, perform and analyze experimental results in a timely manner
Draft and execute validation protocols for analytical methods
Perform and review data analysis and draft reports for analytical method development and validation
Demonstrate ability to correctly analyze data/results and interpret outcome of experiments and to propose appropriate follow-up and supervision
Identifies and troubleshoots analytical problems with instrumentation, general chemistry, test methodology and samples submitted
Perform assigned tasks carefully, safely and on schedule according to SOPs and supervisor instructions
Sets up various instrumentation for testing according to written test methods and with little to no supervision
As needed, troubleshoots laboratory instrumentation
Leads a sample project with assistance
May participate in client level meetings, with approval
May lead and develop other team members
May advise clients on site procedures
May act as a team /project lead supporting scheduling of project tasks and deliverables
Responsible for ensuring compliance with cGMP and other regulatory guidelines
Analyze information for technical correctness and accuracy
Compile, maintain, interpret and extrapolate data on results of analysis and communicate these results to supervisor
Perform routine laboratory procedures in a timely and efficient manner
Strong understanding of analytical techniques
Participate cGMP activities
Provides input on SOPs and client questions
Maintain laboratory equipment and supplies as directed
May support peer-led laboratory investigations process with assistance
Maintain a clean and safe work-space
Maintain laboratory notebook and/or computer files (i.e. LIMS) according to standard, accepted practices
Participate in group and project meetings as required
Enter project hours promptly and update project status on appropriate tracking and/or timekeeping systems
Attend seminars as required
Participate in and comply with all current safety, health and environmental programs
Shows initiative and interest in learning new techniques and tests
Participates in technical discussions and brainstorming sessions
Communicates issues or challenges to senior staff and/or management
May review test data acquired by others and witness others’ notebooks
Assists with and may mentor others regarding writing technical documentation such as OOS, atypical investigations, deviations and CAPAs
Assists with writings standard operating procedures (SOPs), methods, qualification protocols and other standard documents as directed
Provides input on SOPs and client questions
Effectively and routinely provides training
Actively participates in recruiting efforts
Routinely prepares well written and organized development reports
Performs other related duties as assigned
Qualification
Required
S./B.A. Chemistry with 10+ years of experience in related industry or MS with 6+ years related experience or PhD with 2+ years related experience
Working knowledge of experimental design, including chemistry supporting method development
Good grasp of advanced scientific/technical reading, writing and verbal communication skills
Regularly conceives and applies innovative, technical solutions to a variety of problems
Effective independent researcher
Can articulate and evaluate project concepts and strategy
Operates with substantial latitude for independent actions and decisions relating to technical problems and procedures
Recognized as a technical resource in a related area
Expert in related technologies
Demonstrates continued development in a relevant area of CMC
Working knowledge of advanced laboratory techniques
Working exposure to cross functional techniques including organic chemistry
Subject matter expert in one or more instruments (i.e. GC, LC, dissolution, TGA/DSC)
Able to comply to SOPs and have understanding of regulatory compliance
Working knowledge of scientific concepts, principles and procedures
Actively and positively engages with team and supports process improvements
Ability to read and execute compendial methodologies
Strong understanding of current FDA and cGMP regulations
General knowledge of chemistry and scientific calculations
Hands on experience in analytical techniques such as HPLC, GC, etc
Strong computer skills
Ability to operate laboratory equipment and computers
Ability to take direction from experienced scientists and contributes in a team
Ability to effectively train and mentor others
Good problem-solving skills
Good attention to details
Can repeat and follow detailed scientific procedures
Able to clearly present results verbally in group meetings and in written progress reports
Routinely and effectively presenting findings to clients
Good interpersonal skills and is willing to ask questions about procedures and concepts
Aptitude and willingness to gain more skills and knowledge in support of GMP regulations
Good written and verbal communication skills
Familiarity with computer software such as Empower, ChemDraw, Microsoft Word, PowerPoint, and Excel
Aptitude and willingness to gain more skills & knowledge
Good attention to detail and good problem-solving skills
Benefits
Healthcare
Life insurance
Planning for retirement
Company
Cambrex
Cambrex is a small molecule company that offers drug substance, drug product, and analytical services.
1001-5000 employees
H1B Sponsorship
Cambrex has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (21)
2024 (19)
2023 (16)
2022 (15)
2021 (7)
2020 (8)
Funding
Current Stage
Public CompanyTotal Funding
unknown2019-08-07Acquired
1987-10-02IPO
Leadership Team
Tom Loewald
Chief Executive Officer
Robert Green
EVP & Chief Financial Officer
Recent News
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