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Experience with Akta and vMix streaming tools preferred. Content creation responsibilities: * Create original daily reports for KXAN.com, social media and streaming platforms. * Create video-on ...

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Purify conjugates via FPLC/AKTA, TFF, and column chromatography; troubleshoot yield, homogeneity, and stability issues as they arise. * Write clear SOPs and technical reports; train and support ...

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How much do akta jobs pay per hour?

As of Jul 17, 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 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 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 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.

More about Akta jobs
What cities are hiring for Akta jobs? Cities with the most Akta job openings:
What states have the most Akta jobs? States with the most job openings for Akta jobs include:
Infographic showing various Akta job openings in the United States as of July 2026, with employment types broken down into 91% Full Time, 3% Part Time, and 6% Contract. Highlights an 99% Physical, and 1% Hybrid job distribution, with an average salary of $51,238 per year, or $24.6 per hour.
Associate Scientist - Process Development, Downstream

Associate Scientist - Process Development, Downstream

Catalent Pharma Solutions

Madison, WI • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 21 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

50th of 74 rated pharmaceutical


Job description

Associate Scientist - Process Development, Downstream

Position Summary

  • Shift: Monday - Friday 8am - 4:30pm
  • 100% on-site

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

The Associate Scientist - Process Development is responsible for supporting the development and optimization of biologic manufacturing processes, including upstream cell culture and downstream purification activities. This role executes laboratory experiments such as seed train scale-up, bioreactor operations, and protein purification while applying standard statistical methods to analyze data and improve process performance. The Associate Scientist will maintain accurate documentation in accordance with SOPs and GMP practices, support tech transfer to manufacturing, and collaborate cross-functionally with internal teams and external clients to ensure successful project delivery in a fast-paced, client-driven environment.

The role:

  • Execute laboratory experiments supporting upstream process development, including cell bank vial thaws, seed train scale-up, and bioreactor operations
  • Perform cell culture analytical methods and apply platform processes with moderate modification to optimize productivity and product quality
  • Analyze experimental data using standard statistical methods, including Design of Experiments (DoE)
  • Support downstream purification activities, including chromatography (AKTA), filtration, and tangential flow filtration
  • Maintain accurate documentation and batch production records (BPRs) in accordance with SOPs and GDP requirements
  • Collaborate cross-functionally and communicate results with internal teams and external clients to meet project timelines
  • Support lab operations, including equipment maintenance, cleaning, material stocking, and 5S organization
  • Contribute to process development, optimization, and continuous improvement initiatives across client and internal programs

The candidate:

  • Bachelor's degree in a STEM discipline with 1-3 years of related experience
  • Equivalent technical competency may also be demonstrated through completion of a bachelor's degree in Chemical Engineering or a closely related discipline with relevant laboratory, research, or co-op experience
  • Ability to execute laboratory procedures and experiments of moderate complexity with minimal guidance
  • Hands-on experience or exposure to cell culture, bioreactors, or downstream purification (chromatography, TFF, AKTA)
  • Experience with data analysis and statistical methods (e.g., DoE) and ability to interpret results
  • Experience working within GMP/regulatory environments, including SOPs, GDP, and batch record (BPR) documentation
  • Ability to identify out-of-spec data, troubleshoot issues, and support investigations
  • Strong organization, communication, and ability to manage multiple priorities in a fast-paced environment
  • Experience supporting lab operations (equipment maintenance, cleaning, stocking, 5S) and working cross-functionally

Why you should join Catalent:

  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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