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Akta Jobs (NOW HIRING)

Actalent

Scientist II, Protein Modification

Carlsbad, CA

$30 - $40/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Execute protein purification processes using chromatography systems such as ÄKTA and/or Bio-Rad NGC platforms. * Perform tangential flow filtration (TFF) operations for protein concentration and ...

New

MOST

Associate Scientist, Protein Sciences

San Jose, CA · On-site

$115K - $125K/yr

AKTA systems and other chromatographic columns). * Generate target over-expressing cell lines for antibody discovery work. * Develop strategies to express, purify, and analyze proteins for novel ...

Maxonic

Be Seen First

Biochemist I- Purification

San Diego, CA · On-site

$23/hr

  • Medical

  • Dental

  • Vision

  • PTO

AKTA(s), analytical balance, centrifuge, spectrophotometer, nanodrop, UV detector, chart recorder, biosafety cabinet, and pH Meter. * Capable of working on multiple projects simultaneously both ...

New

Jobtailor

Senior CQV Engineer / Validation Lead

Chaska, MN · On-site

$110 - $165/hr

The resource will support qualification activities for laboratory instrumentation, biosafety cabinets, labeling systems, filling and capping equipment, process equipment, bioreactors, AKTA systems ...

New

Bureau Veritas

$28 - $31/hr

AKTA, LC-MS, UPLC, LTQ, QDA analytical instruments are used. This person will assist with training new staff, work on multiple projects simultaneously and stay current with new modifications of ...

Crowdstaffing

Lab Assistant

Madison, WI · On-site

Complete daily routine maintenance of lab instruments (e.g. change AKTA pump rinsing solutions) and address autonomous maintenance problems observed during normal operations. Maintain Kanban of ...

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How much do akta jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for akta in the United States is $24.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.79 and $26.20 per hour, depending on experience, location, and employer.

What are Akta systems?

Akta systems are specialized chromatography instruments developed by Cytiva (formerly GE Healthcare) used primarily for protein purification in research and biopharmaceutical laboratories. These systems automate and optimize the purification process by controlling parameters such as flow rate, pH, and gradient formation. Akta systems are widely used for purifying proteins, antibodies, and other biomolecules, making them essential tools in molecular biology and bioprocessing. Their user-friendly software and flexibility allow scientists to achieve high purity and reproducibility in their workflows.

What are some common challenges faced by Akta professionals when ensuring legal compliance within organizations?

Akta professionals often encounter challenges in keeping up-to-date with frequent changes in legislation and ensuring all company documents and processes are fully compliant. They may also face difficulties in coordinating with various departments to gather necessary information and ensure timely submissions to regulatory bodies. Additionally, balancing multiple deadlines and managing confidential information requires strong organizational skills and attention to detail. Effective communication and continuous professional development are key to overcoming these challenges.

What are the key skills and qualifications needed to thrive as an Akta (Legal Clerk), and why are they important?

To thrive as an Akta (Legal Clerk), you need a solid understanding of legal procedures, document management, and administrative processes, usually supported by relevant legal education or certification. Familiarity with case management software, legal databases, and office productivity tools is crucial. Attention to detail, organizational skills, and discretion are standout soft skills for handling sensitive legal information. These abilities ensure accurate legal documentation, efficient workflow, and the protection of confidential materials in legal environments.

What is the difference between Akta vs Data Analyst?

AspectAktaData Analyst
Required CredentialsTypically requires certification in data management or relevant industry-specific trainingOften requires a bachelor's degree in statistics, mathematics, or related fields; certifications like CAP or Microsoft Data Analyst are common
Work EnvironmentPrimarily in government agencies, legal settings, or organizations managing official recordsIn various industries including finance, marketing, healthcare, working with data sets and reporting tools
Employer & Industry UsageUsed mainly in legal, governmental, or regulatory contextsWidely used across private and public sectors for data analysis and reporting

While both roles involve working with data, Akta typically focuses on managing official records within government or legal settings, whereas Data Analysts work across diverse industries analyzing data to inform business decisions. The choice depends on your industry and career goals.

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AKTA jobs near you
Infographic showing various Akta job openings in the United States as of August 2026, with employment types broken down into 84% Full Time, 15% Contract, and 1% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $51,238 per year, or $24.6 per hour.

Associate Principal Scientist, Bioconjugation

Abzena Inc.

Bristol, PA • On-site

Full-time

Posted 16 days ago

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Bioconjugation Development Associate Principal Scientist is responsible for helping drive bioconjugation efforts in discovery and process development to support Abzena Bristol's scientific and manufacturing operations. This includes conjugation screening, conjugation reaction optimization, downstream purification development and scale-up activities; mentorship, training and potential management of direct reports; take lead on projects and client-facing meetings and updates; support sales and proposals process by providing technical and SME support including the design and costing of project activities as needed.
Responsibilities
  • Drive and support technical execution of R&D bioconjugation activities and successfully deliver client and internal company projects from initial assignment to completion.

  • Hands-on execution of chromatographic purifications (affinity, hydrophobic interaction (HIC), and ion exchange chromatography (IEX)), membrane filtrations (normal and tangential flow filtrations (TFF)), buffer and solution preparation, conjugation reaction work-up.

  • Perform, develop and optimize bioanalytical characterization (HPLC, UPLC, LC-MS, SEC-MALS, colorimetric assays, etc.) of conjugate products.

  • Leverage expertise to aid in the design and management of project plans and conjugation strategies with a focus on improving project completion times.

  • Serve independently as bioconjugation technical lead and subject-matter expert (SME) for internal and external project communications.

  • Training, mentorship, and management of assigned reports.

  • Monitor and assess direct report(s) performance through regular tracking of department based KPIs.

  • SME and technical support for sales and proposals teams, including client facing scoping calls, bid defenses and proposal generation.

  • Help lead technical transfer of bioconjugation processes to Abzena's bioconjugation manufacturing group including training, risk assessment, gap assessments and batch record writing and review according to ICH and FDA guidelines.

  • Authoring and reviewing relevant documentation including laboratory notebooks, process development reports, protocols, batch records, SOPs, technical presentations.

  • Provide on-the-floor SME and technical support during complex manufacturing operations as needed.

  • Coordinate activities with QA/QC and Management for development of tox and GLP batches.

  • Maintain strong technical understanding of advancements in bioconjugation/bioprocessing through literature searches and review.

  • Participate in the hiring process by screening and interviewing candidates.

  • Operate to the highest ethical and moral standards.

  • Comply with Abzena's policies and procedures.

  • Communicate effectively with clients, supervisors, colleagues and staff.

  • Participate effectively as a team player in all aspects of Abzena's business.

  • Adhere to quality standards set by regulations and Abzena policies, procedures, and mission.

  • Perform other duties as assigned.

  • Contribute to assigned laboratory operations including instrument and equipment operations, material shipment preparation, consumables procurement.

Qualifications
  • A PhD in chemistry, bioorganic chemistry, chemical biology or similar with >7 years industry experience in biotherapeutic conjugate development or bioconjugation.

  • Demonstrated experience applying and optimizing state-of-the-art bioconjugation or bioorthogonal chemistry techniques to produce conjugates (ADCs, AOCs/ARCs, PDCs, DACs, etc.) at various scales (mg-gram scales)

  • Thorough, hands-on experience with small-scale and preparative chromatography systems (AKTA Pilot, AKTA Ready, AKTA Explorer, etc.) for purification of biomacromolecules (antibodies, fusion proteins, carrier proteins, viruses, viral vectors, or other biologics).

  • Expertise in normal flow filtrations and tangential flow filtrations (TFF or UF/DF).

  • Knowledge of strategies for the optimization of bioprocesses and experimental design (DoE).

  • Expertise with quantitative determination of scalable process parameters for normal flow filtrations, tangential flow filtrations, and preparative chromatographic separations.

  • Knowledge of cGMP manufacturing operations and GxP principles.

  • Experience with protein bioanalytical techniques (HPLC, LC-MS, CE-SDS, UV-spectrophotometry, etc.)

  • Experience with large scale bioprocess equipment (pallet tanks, pumps, biowelders, biosealers, bio-rockers, single-use assemblies).

  • Prior leadership experience required.

Travel between Abzena sites (Bristol PA, San Diego CA, Cambridge UK) as needed.
Physical Requirements
  • Ability to stand for 1-2 hours at a time, sit for 2 to 3 hours at a time.

  • Frequently lift and or move objects up to 30 pounds.

  • Stand/walk during entire length of shift.

  • Use arms, hands and fingers to handle, feel or reach.

  • Ability to climb, balance, stoop, kneel, crouch, or crawl.

  • Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus

FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

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