Associate Scientist / Sr. Associate Scientist

Planet Pharma; Cambridge (MA); On-site; USD 62,000 - 76,000; Full time

Job summary

Planet Pharma in Cambridge, MA, is seeking an experienced Scientist to join the Oligonucleotide Purification Development team. The role focuses on developing robust purification processes for oligonucleotides and peptides, with exposure to manufacturing processes for clinical and commercial therapeutics.

You will lead purification development, scale-up activities, and contribute to tech transfer and IND regulatory documentation, while mentoring new staff and collaborating across functions.

Qualifications

• Proven record of planning and executing projects and experiments.
• Demonstrated technical proficiency and creativity in developing purification technologies.
• Lab experience in purification of proteins, peptides and/or DNA/RNA using chromatography and UF/DF.

Responsibilities

• Develop and characterize purification processes for oligonucleotides and peptide drug therapies.
• Utilize multiple modes of chromatography and UF/DF; learn cleavage/conjugation/hybridization steps.
• Collaborate cross-functionally to improve process understanding and manage team activities.
• Document laboratory work in development reports and lead pilot scale activities.
• Scale-up and technology transfer of oligonucleotide processes to pilot and GMP facilities; contribute to IND sections.

Skills

Project planning

Purification expertise

Chromatography

UF/DF

HPLC/UV-Vis

AKTA/Unicorn

DoE

Cross-functional collaboration

Education

Biochemistry degree

Chemical Engineering degree

Chemistry degree

Tools

AKTA purification systems

Unicorn software

Job description

Pay range: 45-55/hr
*depending on exp

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 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.

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:

• Proven record of successfully planning and executing projects and experiments. Excellent verbal andwritten 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

Education:
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.