About Astellas Gene Therapies
Astellas Gene Therapies is an Astellas Center of Excellence developing genetic medicines for patients with rare, life-threatening diseases. Based on our innovative approach to developing genetic medicines, as well as our industry-leading internal manufacturing capability and expertise, we have become the Astellas Center of Excellence for their newly-created Genetic Regulation Focus Area. We are currently exploring three gene therapy modalities: gene replacement, exon skipping gene therapy, and vectorized RNA knockdown, with plans to expand our focus and geographic reach under Astellas. We are based in San Francisco, with manufacturing and laboratory facilities in South San Francisco and Sanford, North Carolina. For more information, please visit our website: www.astellasgenetherapies.com
About Astellas
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are promoting the Focus Area Approach that is designed to identify opportunities for the continuous creation of new drugs to address diseases with high unmet medical needs by focusing on Biology and Modality. Furthermore, we are also looking beyond our foundational Rx focus to create Rx+® healthcare solutions that combine our expertise and knowledge with cutting-edge technology in different fields of external partners. Through these efforts, Astellas stands on the forefront of healthcare change to turn innovative science into value for patients. For more information, please visit our website at https://www.astellas.com/en.
Our Values:
Be BOLD (Find a Way)
Care Deeply – for our patients, each other and our work
#GSD (Get Stuff Done)
What is the catalyst for you in your professional career? Are you ready to be a part of a bold, innovative company, to make a change and to make a difference? Listed below is a current opening for a smart, driven, experienced, and just plain nice individual who wants to join us and be a part of our journey.
The Role
The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials, and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines.
Responsibilities
Support Quality Control testing of drug substances, raw materials, and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines
Perform bioburden, endotoxin, pH/Conductivity, and other tests as needed
Perform viable air, non-viable particulate, surface/swab environmental monitoring (EM) of manufacturing areas
Perform sampling and testing for gas, utilities, and purified water
Perform growth promotion/media sterility check, Gram staining and microbial cryopreservation
Perform plate reading, generate microbial isolates, and shipping of isolates for identification
Receive, unpack, and organize supplies for QC areas
Revise SOPs, Forms, and approved documents
Initiate deviation and OOS investigations, as encountered
Support Fill and Finish operations
Assist in data trending and summarization
Perform routine cleaning, schedule equipment preventative maintenance, and organization of laboratory areas in accordance with cGMP requirements
Assist in performing laboratory Investigations
Support Quality Control Microbiological testing of drug substances, raw materials, and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines.
Required Qualifications
Bachelor’s Degree in chemistry, biology, or microbiology with 0-3+ years’ relevant microbiology laboratory experience in Pharmaceutical/Biotech.
Excellent knowledge of Aseptic technique and common microbiological testing
Knowledge of relevant, compliance and guidance documents
Must be able to gown into cleanrooms in support of testing and manufacturing activities
Good documentation (ALCOA +) and data organization
Detail oriented and willingness to learn and follow instructions
Interpersonal skills and ability to contribute to the success of a team
Preferred
Proven history of working in a fast-paced team environment, time management, and meet deadlines.
Team player with the ability and willingness to support other colleagues in the Quality Control department. This support may include future cross training with analytical assays as needed
Models our Core Values: Be Bold, Care Deeply, #GetStuffDone – is experienced as someone who exemplifies the culture we want to create; operates with transparency; is trusted
Working Conditions
Must be willing to work second shift, rotating shifts, overtime, weekends, and holidays, as required
Must be proficient in use of computer, particularly Microsoft Word and Excel programs, and be able to sit/stand and be gowned inside the cleanroom for extended periods of time. Some lifting required (not more than 50 lbs.). Routinely able to stand, walk, kneel, and crouch while performing sampling, such as environmental monitoring.
Ability to tolerate the smell of Gram-negative organisms and disinfectants (i.e. 1% bleach, SporeKlenz) may be needed. Use of a respirator may be required. Exposure to biohazards and viruses.
Salary Range: $61,500-82,000 (NOTE: Final salary could be more or less, based on experience)
Benefits
Medical, Dental and Vision Insurance
Generous Paid Time Off options, including Vacation, Sick time, plus national holidays including Heritage Days, and Summer and Winter Breaks
401(k) match and annual company contribution
Company paid life insurance
Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
Long Term Incentive Plan for eligible positions
Referral bonus program
All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.
#LI-TR1
Category South San Francisco TC
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability/Protected Veterans