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... brave science. For more information, visitneurocrine.com, and follow the company onLinkedIn ... Develops and executes instrumental methods of analyses for development compounds, drug substances ...
... science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and ... Develops and executes instrumental methods of analyses for development compounds, drug substances ...
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... brave science. For more information, visitneurocrine.com, and follow the company onLinkedIn,X ... Responsible for leading analytical development activities for multiple projects to support drug ...
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Expert knowledge and understanding of analytical chemistry, separation sciences, and a thorough understanding of bioprocess as well as formulation development * Extensive experience and expertise ...
Senior Scientist, Analytical Development
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The Senior Scientist position within Analytical Development leads small molecule analytical activities within a growing, dynamic Pharmaceutical Development organization. They will collaborate with ...
Senior Scientist, Analytical Development
$151K - $161K/yr
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Associate Scientist Analytical Development information
See salary details
$18.75 - $22.27
6% of jobs
$22.27 - $25.79
12% of jobs
$27.48 is the 25th percentile. Wages below this are outliers.
$25.79 - $29.31
14% of jobs
$29.31 - $32.82
13% of jobs
The median wage is $33.88 / hr.
$32.82 - $36.34
16% of jobs
$39.79 is the 75th percentile. Wages above this are outliers.
$36.34 - $39.86
14% of jobs
$39.86 - $43.38
11% of jobs
$43.38 - $46.90
6% of jobs
$46.90 - $50.42
5% of jobs
$50.42 - $53.93
1% of jobs
$53.93 - $57.45
1% of jobs
$18
$35
$57
How much do associate scientist analytical development jobs pay per hour?
What are the key skills and qualifications needed to thrive as an Associate Scientist Analytical Development, and why are they important?
What are some common challenges an Associate Scientist in Analytical Development might face when working on new drug formulations?
What does an Associate Scientist in Analytical Development do?
What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?
| Aspect | Associate Scientist Analytical Development | Associate Scientist Quality Control |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experience | Bachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing |
| Work Environment | Research and development labs, method development, process optimization | Quality control labs, testing, sample analysis, compliance with regulations |
| Employer & Industry Usage | Pharmaceutical, biotech companies, focus on method development | Pharmaceutical, biotech companies, focus on product testing and quality assurance |
Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 24 days ago
Job description
WORKING AT GENEZEN
Many people have worked in environments where you feel like just another nameless part of an enormous machine. Genezen is different. We want our employees to be innovative, collaborative problem solvers who are dedicated to meeting the challenges of working at a fast-growing company. We are dedicated to empowering our employees to be their best and making Genezen a rewarding place to work. Every employee contributes to the success of the company and you can be part of that team.
JOB SUMMARY
Lead the establishment of methods in the Analytical Development (AD) and Quality Control lab from the bench. This individual will be accountable for development and validation of analytical and QC assays, equipment specification and selection and the direction of analytical method transfer from the analytical development lab to the QC lab while operating under cGMP standards. The person is expected to work collaboratively with the team to establish and implement best regulatory, laboratory practices and to lead the execution of complex experiments. The position requires expertise in potency and other cell based assays, ddPCR/qPCR, and ELISA. Considerable expertise with experimental design toward method qualification and validation per ICH guidelines in a phase appropriate manner. Considerable expertise with technical writing of protocols, SOPs, and technical reports. Experience with biophysical characterization methods including HPLC, LC-MS, CE-SDS etc. Direct line management experience is required.
JOB RESPONSIBILITIES
- Experience with AAV assay development is critical
- Expert in method qualification/validation experimental design per ICH guidelines
- Experience with specification setting for complex biologics
- Expert in potency method development
- Expert in ddPCR/qPCR from primer design and optimization to implementation
- Expert with ELISA assay development
- Experience in HPLC based methodology development and establishment including with the use of CAD and MALS detectors for use in the characterization of AAV vectors
- Maintain familiarity with other current analytical and bioassay methods, including Flow cytometry
- Maintain familiarity with current equipment used in Analytics lab
- Help management evaluate new technology and bring new platforms in-house
- Qualify/validate analytical methods to support cGMP testing
- Help facilitate tech transfer of analytical and bioassays from clients to AD lab and from AD lab to QC lab
- Supervise and train AD Associates and AD Technicians and work closely with other departments, assisting in project planning
- Support the establishment of electronic record keeping systems for site; e.g. LIMS or ELN
- Analyze regulatory authorities' programs, guidance documents, and activities in areas relevant to testing of biological products
- Work as a team with process development, manufacturing, quality assurance and quality control departments as needed
- Advise site and quality management of potential and actual actions that could adversely affect the business, represent quality exposures, or represent opportunities to be pursued
- Execute research timelines to meet program and corporate objectives
- Deal with abstract and concrete variables in situations where only limited standardization exists
- Maintain high quality deliverables and open communication, creating a collaborative working environment
- Contribute to collaborative, creative and rigorous culture of scientific discovery
- Provide weekly reports to department head in 1:1 environment
SPECIAL JOB REQUIREMENTS
- People training and leadership skills
- Ability to maintain multiple projects and timelines
- Excellent verbal and written communication skills
- Extremely high levels of initiative, adaptability, tenacity and troubleshooting skills
KNOWLEDGE, SKILLS AND EXPERIENCE
EDUCATION / CERTIFICATIONS / LICENSES
Essential/Desired
BS in scientific/technical discipline
Essential
ON-THE-JOB EXPERIENCE
5-6 years experience post graduation (with PhD), 6-8 years experience post graduation (with Masters), 8-12 years experience post graduation (with Bachelors)
Essential
2-4 years of CRO/CDMO experience in design, development and execution of bioanalytical methods (i.e. method development, qualification, validation and transfer). Methods include, but are not limited to: Potency for AAV vectors, cell based assays, ELISA, ddPCR, qPCR, HPLC using UV-Vis, CAD, and MALS detectors, and flow cytometry-based assays.
Essential
Expertise in molecular biology in the characterization of AAV particles and associated impurities.
Essential
Experience with documentation and reporting of results using electronic lab notebooks
Essential
SKILLS / ABILITIES
People training and leadership skills
Essential
Ability to maintain multiple projects and timelines
Essential
Excellent verbal and written communication skills
Essential
Extremely high levels of initiative, adaptability, tenacity and troubleshooting skills
Essential
Pay Range:
- The annual salary range for the Senior Scientist is $120,000-$150,000.
Work Environment
- Frequently required to work in BSL2 environment with personal protective equipment/aseptic gowning
- Occasionally exposed to moving mechanical parts, toxic or caustic chemicals, hazardous waste, and similar hazards associated with pharmaceutical lab facilities
Movement
- Frequently required to stand; sit; use hands to finger, handle, or feel; reach with hands and arms
- Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl
Lifting
- Frequently lift and/or move up to 10 pounds
- Occasionally lift and/or move up to 25 pounds
Vision
- Frequently utilize close vision and the ability to adjust focus
Communication
- Frequently required to communicate by talking, hearing, using telephone and e-mail
GENEZEN'S CURES VALUE-BASED COMPETENCIES
Committed to Science
We are committed to scientific excellence, staying current with industry developments, making data-driven decisions, and pursuing innovation to advance healthcare.
Urgency in action for the patients
We operate with urgency and a commitment to delivering timely treatments to patients by accelerating our partners' programs.
Resilience & Grit in operations
We are committed to overcoming challenges, learning from failures, and persistently striving for success.
Execute with Excellence & Integrity
We are dedicated to delivering quality results and upholding ethical principals.
Solutions driven for our partners
We are committed to being a proactive, collaborative, creative and open-minded partner.
GENEZEN'S BENEFITS
- Paid vacation days, amount based on tenure
- Paid sick time
- 10 observed holidays + 2 floating holiday + 1 volunteer day
- 401(k) plan with company match up to 6% of salary, vested immediately
- Share Appreciation Rights
- Choice of several healthcare plans
- FSA and HSA programs
- Dental & vision care
- Employer-paid basic term life/personal accident insurance
- Voluntary disability, universal life/personal accident insurance
- Accidental Death & Dismemberment (AD&D) Insurance
ADDITIONAL DETAILS
- Nothing in the job description for this role restricts management's right to assign or reassign duties and responsibilities to this job at any time.
- This position requires a criminal background check.
- Genezen is an Equal Opportunity Employer.
- Genezen participates in EVerify.
- Genezen is interested in every qualified candidate who is eligible to work in the United States; however, we are not able to sponsor visas.
Genezen has operates two locations: one in Fishers, Indiana and the second in Lexington, Massachusetts.
Fishers is a suburb of Indianapolis. Fishers was named the #1 place to live in the US by Money Magazine in 2017 for its livability, safety and entrepreneurship. Fishers is one of the fastest growing communities in Indiana and is dedicated to supporting a high quality of life for all its residents. Nearby Indianapolis is home to professional and college sports teams, the Indy 500, a growing art community and the world's largest children's museum--to name just a few reasons why this area is a great place to live.
Lexington, Massachusetts, located just northwest of Boston, is renowned as a historic suburb with a rich cultural heritage. It boasts picturesque New England charm, tree-lined streets, and a vibrant community. Known for its pivotal role in the American Revolution, Lexington offers visitors and residents alike a blend of historical landmarks, modern amenities, and a strong sense of community pride.
About Genezen Laboratories
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
Indianapolis, IN, US
Year founded
2014