This job is closed
Applications are no longer available for this announcement. Explore current related opportunities below.
Job description
At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.
What You'll Do
The Associate Director, Analytical Development and Quality Control will support analytical development and QC operations for clinical development and commercialization of Kailera’s pipeline compounds. The individual will provide technical expertise and will work closely with cross‑functional stakeholders to ensure end‑to‑end drug development and manufacturing activities are executed seamlessly and in alignment with the company’s integrated development plans and program timelines.
Required location: Waltham, MA (hub‑based, onsite 3‑4 days per week)
Responsibilities
Support analytical development and QC activities related to characterization of peptide drug substances and drug products from early‑stage clinical development through commercialization
Maintain current knowledge in analytical methods and control strategies supporting a variety of molecule platforms and dosage forms
Support development of analytical methods that support Kailera’s product pipeline, including analytical transfers and troubleshooting in CDMO laboratories
Provide input for developing and implementing analytical development strategies, including managing execution of functional activities in support of clinical development, regulatory filings (IND/NDA/MAA), product approvals, and commercialization
Support authoring of relevant CMC sections to enable global regulatory filings
Participate on cross‑functional CMC teams for the project(s) assigned to ensure adequate development and execution of CMC plan/strategies as needed
Communicate CMC project status to key stakeholders cross‑functionally and assist in driving decision‑making
Collaborate with cross‑functional line functions to ensure CMC and program goals are met
Travel to CDMOs and other service providers as needed for vendor technology transfers and analytical activities oversight
Required Qualifications
A bachelor’s degree and 10+ years of experience in the pharmaceutical/biotech industry with experience in all phases of innovative drug development and commercial launch in accordance with global CMC regulatory filings (IND/NDA/MAA, etc.)Or an advanced degree with 5+ years
Knowledge of peptide chemistry is required
Demonstrated project and cross‑functional team participation
Experience in authoring regulatory documents
Knowledge of drug development activities with respect to cGMP, quality systems, ICH guidelines, global regulatory requirements, and USP, EP, JP, and CHP requirements
Experience with oversight of the analytical activities at CDMOs and/or CTLs
Sound problem‑solving skills with technically driven decision‑making ability
Effective written and verbal communication and interpersonal skills
Innovative team‑player with high energy for our dynamic company environment
Preferred Qualifications
Knowledge and experience in analytical development of peptide therapeutics (DS and DP)
Knowledge and experience in analytical development of injectable products, and associated control strategies
Education
A Bachelors degree with 10+ years or an advanced degree with 5+ years of relevant experience
Degree in Analytical Chemistry, Organic Chemistry, Physical Chemistry, Pharmaceutical Sciences, or closely related field.
Additional Information
This position requires some travel to domestic and international destinations
This position requires working in environments where there may be specific gowning or dress code requirements
Salary Range
$155,000 – $190,000 USD
Benefits
For Full Time Roles: This range represents the company’s good‑faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year‑end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants—because your well‑being and future matter to us.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy‑related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E-Verify
Kailera Therapeutics, Inc. uses E‑Verify to confirm the identity and employment eligibility of all new hires.
#J-18808-Ljbffr
Worksite address
waltham, MA, 02254, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.