Skip to content

Open nowPosted 13 days ago

Process Development Associate

MyCareersFuture94,028 open roles

Pay
SGD 3,000 – SGD 5,000 a month
Where
West, Singapore
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowProcess Development AssociateMyCareersFuture · West, Singapore
  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on MyCareersFuture's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

7.7% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.6%1 day
  2. 3.3%3 days
  3. 7.7%7 days
  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 13 days ago

The posting

The Opportunity

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017. Our company is a contract research development and manufacturing organization that are

founded and deeply rooted by scientists that enables fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work involves in the field of emerging biotechnologies where we are developing cells as a final product or leveraging them as cellular factories to produce target modalities. Our first commercial breakthrough success is being first in the world to be certified by established food regulatory body for commercial production cultivated/cell-based meat. Our second milestone focuses on manufacturing engineered extracellular vesicles to support a Phase I oncology clinical trial in US.

We have established an end-to-end, integrated suite of capabilities that encompasses cell line development, upstream cultivation of cells, downstream purification and analytical testing. Operating under cGMP compliance, this centralized infrastructure supports both drug substance and drug product manufacturing across a diverse range of biologic modalities.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

Esco Aster.

One World Biosolutions for One Health.

The Scope

You will be part of Esco Aster’s scientific division and contribute to the company’s CDMO mission and objectives. You will perform research and process development activities, mainly in support of the production of biologics, in collaboration with internal and external stakeholders, clients and partners.

Primary Work Location: Ayer Rajah Crescent, Singapore

Desired profile of candidate

Technical competency:

1. Demonstrated competency in designing, optimization/improvements and troubleshooting laboratory scale experiments on either two major areas, which include:

· Cultivation of mammalian cells and analysis of the cellular mechanism in promoting growth and production of biologics.

· Purification of various biologics modalities produced from cells using processes such as tangential flow filtration, chromatography and filtration.

2. Support process development and process characterization studies to scale up mammalian cell culture and/or purification processes for technology transfer into cGMP manufacturing processes.

3. Ability to collate, analyse and interpret the experimental data to define subsequent steps and contributing to the scientific and operational improvements to the overall manufacturing process.

4. Drafting and documentation of process SOP, batch records and workflow diagram for GMP manufacturing operations.

The candidate should also:

  • Understand and be willing to work under cGMP manufacturing environment during the process development stage.
  • Meticulous and organized in scheduling experimental assays, documentation of experimental reports, and drafting protocols in accordance with Good Documentation Practice (GDP) and cGxP requirements.
  • Take ownership of experimental timelines by ensuring that all experiments are executed on schedule, and results are systematically compiled and submitted timely to all relevant stakeholders for review.
  • Ability to communicate and explain experimental results effectively with internal stakeholders and identify logical next steps of the experiment.
  • Demonstrates a positive and proactive attitude and towards guidance. Willingness to learn new process techniques and demonstrate interest to continuous deepen skill expertise.
  • Demonstrate collaborative efforts with cross functional teams to support the establishment of process in GMP settings.
  • Perform tasks in accordance with applicable regulations and site safety requirements.
  • Undertake other tasks as assigned based on project needs. Able to maintain schedule flexibility to accommodate experimental timepoint and workflow demands.

Requirements

· Bachelor/Masters degree in Biology,Chemistry, Pharmaceutical Sciences or related science.

· Experience with Good Laboratory Practices(GLP) and Good Manufacturing Practices (GMP) will be an advantage.

· Proficient in MS Office Suite (MicrosoftWord, PowerPoint, Excel).

· Experience in cultivation of mammalian cellsin laboratory scale and in bioreactor systems.

· Experience in downstream processingtechniques such as tangential flow filtration, chromatography, ultrafiltration.

· Strong computer, scientific, and organizational skills.

· Excellent communication (oral and written) and attention to detail.

· Strong team player, develop positive relationship with a strong set of interpersonal skills.

· Ability to work independently and as part of a team, self-motivated, adaptable, and has a positive attitude.

· Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.

· Ability to work on complex assignments independently and take a high degree of initiative to resolve issues

· A friendly and pleasant disposition.

Interested candidates should provide a CV [email protected] and are encouraged to provide a cover letter detailing the following:

· Their perspective on the key challenges of this role

· How they will contribute to this role with their skillset and experience

· Their approach to shape and grow within the role

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against MyCareersFuture's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.
  3. We apply on MyCareersFuture's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.
  4. Every reply, sorted

    MyCareersFuture's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.
  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

By hand5–10
With CV Rocket100
applications a day

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.