Analytical R&D Lead - Pharmaceutical / Nutraceutical at CONTRACT PHARMACAL CORP

Town of Smithtown, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

14 May, 26

Salary

135000.0

Posted On

13 Feb, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Method Development, Validation, cGMP, Technical Writing, Leadership, Mentoring, HPLC, UPLC, LC-MS, GC-MS, ICP-OES/MS, FTIR, Regulatory Submissions, CMC, ANDA, Project Management

Industry

Pharmaceutical Manufacturing

Description

Description Position Summary We’re looking for a senior analytical leader to serve as the right hand to our Vice President of AR&D – a role designed for someone who thrives at the intersection of science, leadership, and execution. This position acts as the connective tissue between AR&D leadership and laboratory scientists, ensuring analytical development work is technically sound, clearly documented, inspection-ready, and aligned with business priorities. You’ll bring broad analytical expertise, strong technical writing skills, and a leadership mindset that elevates both people and programs. Job Type: Full-Time Location: Hauppauge, NY Level: Manager, Sr Manager, or Director Works Hours: Monday – Friday, 8:00AM – 4:00PM EST Pay Range: $105,000 - $135,000 per year, depending on experience and level Start Date: ASAP What makes this role exciting Act as a trusted partner to the VP of AR&D with meaningful influence on strategy, priorities, and execution A chance to shape how analytical development is executed and communicated, not just reviewed High visibility across Formulation R&D, QA, QC, Regulatory Affairs, and Project Management Blend of technical depth, leadership, and operational ownership – ideal for someone ready to expand beyond the bench Opportunity to mentor and elevate scientists while ensuring work is inspection-ready and submission-quality Exposure to CMC and ANDA-enabling activities that directly impact product success Why Join CPC? At CPC, you’ll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact. Requirements Responsibilities In this role, you will: Act as a technical and operational bridge between AR&D leadership and laboratory teams Provide scientific oversight for analytical method development, validation, transfer, and investigations Ensure analytical deliverables are executed on schedule and aligned with overall project timelines and business priorities Prepare and review methods, protocols, reports, and regulatory-facing documentation Partner cross-functionally to support CMC and submission-enabling activities Help translate strategy into clear priorities, timelines, and execution Mentor scientists, strengthen technical rigor, and reinforce a culture of quality and accountability Education & Experience BS, MS, or Ph.D. in Chemistry, Pharmaceutical Sciences, or a related scientific discipline Manager level: 5+ years of experience in analytical development Senior Manager: 7+ years of experience in analytical development Director level: 10+ years of progressive experience in analytical development Prior experience supporting method development, validation, and regulatory submissions (CMC/ANDA) required Experience leading or mentoring scientific teams strongly preferred Skills, Knowledge & Abilities Broad, working knowledge of analytical techniques, including chromatography (HPLC, UPLC, LC-MS, GC, GC-MS, ICP-OES/MS, TLC/HPTLC), spectroscopy (UV-Vis, FTIR), and classical/wet chemistry Strong understanding of cGMP, data integrity principles, FDA and ICH guidelines Exceptional technical writing skills with the ability to produce clear and concise documentation Ability to translate complex scientific concepts for both technical and non-technical stakeholders Proven leadership skills with the ability to influence without authority and bridge leadership and bench-level execution Strong organizational, prioritization, project management, communication and problem-solving capabilities Proficiency with standard business and documentation tools (e.g., Microsoft Office)

Responsibilities

This role serves as the technical and operational bridge between Analytical R&D leadership and laboratory teams, providing scientific oversight for method development, validation, transfer, and investigations. The lead ensures analytical deliverables meet project timelines and business priorities while preparing and reviewing regulatory-facing documentation.