Scientist – Oligonucleotide/Peptide

Ipro Networks Pte. Ltd.; Cambridge (MA); On-site; USD 110,000 - 135,000; Full time

Job summary

IntelliPro is seeking a Scientist – Oligonucleotide/Peptide purification in Cambridge, MA to develop robust purification processes for a growing pipeline of oligonucleotide and peptide therapeutics. The role includes scale-up, tech transfer, and cross-functional collaboration across synthesis, analytics, and manufacturing.

The ideal candidate has hands-on purification experience (AKTA/U Unicorn), strong communication, and a track record of delivering development reports and pilot-scale

Qualifications

• Bachelor’s degree in Biochemistry, Chemical Engineering, Chemistry or related life science field with 2-4 years industry experience (or master’s degree with 0-2 years of industry experience).
• Senior Associate Scientist: Bachelor’s degree in Biochemistry, Chemical Engineering, Chemistry or related life science field with 4 years industry experience (or master’s degree with 2 years of industry experience).

Responsibilities

• Develop and characterize purification processes for a rapidly expanding pipeline of oligonucleotides and peptide drug therapies.
• Utilize chromatography and UF/DF; learn purification steps for oligonucleotide and peptide platforms.
• Collaborate cross-functionally to improve process understanding and manage team activities.
• Document development work and lead pilot scale activities; contribute to IND regulatory sections.

Skills

Project planning

Communication

Purification technology

Time management

Education

Bachelor’s in Biochemistry/Chemical Engineering/C**hemistry

Master’s degree (optional)

Tools

AKTA purification systems

Unicorn software

Job description

Job Title: Scientist – Oligonucleotide/Peptide

Location: Cambridge, MA 02142

Duration: 10/27/2026 to 04/26/2027 contract to permanent hire

Pay rate: $55.38/hr. on W2

Summary:

We are seeking a highly motivated and creative individual with some process development experience to join our Oligonucleotide/Peptide Purification Development team. This position provides an exciting opportunity to develop robust, high purity, state of the art processes for the purification of oligonucleotides. This position provides an exciting opportunity to gain hands-on experience and exposure to the design and development of manufacturing processes for clinical and commercial therapeutics. We are looking for someone who is passionate for exploring novel scientific ideas and play a key role in developing new cutting-edge technologies with a vision to push client’s state-of-art science in oligonucleotide and peptide purification that can ultimately impact patient lives.

Job Description:

• This role in the oligonucleotide development modality is responsible for purification development including process development, process characterization, scale-up, for all unit operations (chromatography, detritylation, UF/DF) with some guidance. This position is expected to learn our oligonucleotide platform and develop our peptide platform while exploring non-platform and novel purification steps.
• They should have knowledge of the manufacturing facilities and equipment, contribute to tech transfer activities, document review, provide on-the-manufacturing floor support, troubleshooting and authoring CMC section of INDs. These activities can include early and late-stage process characterization and robustness studies.
• This position will act as a subject matter expert on purification processes to facilitate interactions internally within the oligonucleotide organization (synthesis, drug product, analytical) as well as cross functionally (with Research/Manufacturing/MS project and tech transfer teams).
• The ability to write development reports, training/mentoring of new employees, lead pilot scale activities and collaborate across teams or lead small, focused initiatives are important.
• Some independent work is expected (e.g., root cause investigations, evaluation of processes with some guidance from the supervisor.

Key Responsibilities:

• Develop and characterize purification processes for a rapidly expanding pipeline of new oligonucleotides and peptide drug therapies.
• The individual will utilize multiple modes of chromatography and ultrafiltration and learn chemical cleavage/conjugation/hybridization steps.
• Investigate new purification technologies that seek to enhance purity, process robustness and/or productivity of our existing oligonucleotide platform process.
• Collaborate cross-functionally with other groups to improve process understanding and manage team activities.
• Document laboratory work in development reports, training/mentoring of new employees, and lead pilot scale activities.
• Scale-up and technology transfer oligonucleotide processes into our pilot and GMP manufacturing facilities and participate in writing regulatory sections for INDs

Qualifications:

Education and Experience

• Associate Scientist 3/Engineer 2: Bachelor’s degree in Biochemistry, Chemical Engineering, Chemistry, or related life science field with 2-4 years industry experience (or master’s degree with 0-2 years of industry experience) is required.
• Senior Associate Scientist: Bachelor’s degree in Biochemistry, Chemical Engineering, Chemistry or related life science field with 4 years industry experience (or master’s degree with 2 years of industry experience) is required.

Technical Knowledge and Skills

• Proven record of successfully planning and executing projects and experiments.
• Excellent verbal and written communication skills.
• Demonstrated technical proficiency and creativity in developing innovative technologies/approaches in purification. Excellent organizational, communication, and time management skills.
• Lab experience in purification of proteins, peptides and/or DNA/RNA using column chromatography (e.g., Ion exchange, Hydrophobic Interaction, and/or Reversed phase) and UF/DF.
• Some hands-on experience in analysis of proteins, peptides or DNA/RNA, preferably using both HPLC and UV/Vis spectroscopy. Experience using AKTA purification systems and Unicorn software and use of statistical design (DoE) are a plus. Experience in statistical analysis is also a plus.
• Motivated to work and communicate both individually and within teams

About Us:

Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.

IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants.

Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.

Compensation:

The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.